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esv2421683

  • Variant Calls:34
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,172

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 159 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):160,207,873-160,217,044Question Mark
Overlapping variant regions from other studies: 159 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):160,628,905-160,638,076Question Mark
Overlapping variant regions from other studies: 63 SVs from 16 studies. See in: genome view    
Submitted genomic160,548,895-160,558,066Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2421683RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6160,207,873160,217,044
esv2421683RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6160,628,905160,638,076
esv2421683Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr6160,548,895160,558,066

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
essv5003951deletionNA19041SNP arraySNP genotyping analysis1140
essv5006575deletionNA21317SNP arraySNP genotyping analysis1142
essv5007617deletionNA19431SNP arraySNP genotyping analysis1157
essv5015342deletionNA21436SNP arraySNP genotyping analysis1143
essv5019869deletionNA19404SNP arraySNP genotyping analysis1134
essv5025963deletionNA21309SNP arraySNP genotyping analysis1137
essv5027323deletionNA21583SNP arraySNP genotyping analysis1149
essv5030128deletionNA21517SNP arraySNP genotyping analysis1134
essv5030774deletionNA19468SNP arraySNP genotyping analysis1130
essv5032578deletionNA19226SNP arraySNP genotyping analysis1156
essv5036758deletionNA19044SNP arraySNP genotyping analysis1157
essv5038118deletionNA21403SNP arraySNP genotyping analysis1131
essv5039685deletionNA20333SNP arraySNP genotyping analysis1146
essv5041347deletionNA19035SNP arraySNP genotyping analysis1121
essv5048344deletionNA21574SNP arraySNP genotyping analysis1135
essv5060706deletionNA21580SNP arraySNP genotyping analysis1136
essv5061230deletionNA19096SNP arraySNP genotyping analysis1138
essv5063343deletionNA18510SNP arraySNP genotyping analysis1141
essv5068365deletionNA21723SNP arraySNP genotyping analysis1138
essv5087087deletionNA19373SNP arraySNP genotyping analysis1138
essv5089183deletionNA21352SNP arraySNP genotyping analysis1160
essv5091877deletionNA21527SNP arraySNP genotyping analysis1133
essv5104273deletionNA21473SNP arraySNP genotyping analysis1163
essv5111988deletionNA21632SNP arraySNP genotyping analysis1142
essv5114788deletionNA21307SNP arraySNP genotyping analysis1140
essv5123797deletionNA19819SNP arraySNP genotyping analysis1139
essv5132067deletionNA19318SNP arraySNP genotyping analysis1126
essv5133421deletionNA21363SNP arraySNP genotyping analysis1150
essv5143871deletionNA18925SNP arraySNP genotyping analysis1128
essv5144936deletionNA21308SNP arraySNP genotyping analysis1136
essv5151512deletionNA20332SNP arraySNP genotyping analysis1143
essv5155585deletionNA20773SNP arraySNP genotyping analysis1124
essv5155910deletionNA18923SNP arraySNP genotyping analysis1135
essv5158450deletionNA19391SNP arraySNP genotyping analysis1130

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5003951RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5006575RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5007617RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5015342RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5019869RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5025963RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5027323RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5030128RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5030774RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5032578RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5036758RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5038118RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5039685RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5041347RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5048344RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5060706RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5061230RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5063343RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5068365RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5087087RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5089183RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5091877RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5104273RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5111988RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5114788RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5123797RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5132067RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5133421RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5143871RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5144936RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5151512RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5155585RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5155910RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5158450RemappedPerfectNC_000006.12:g.(?_
160207873)_(160217
044_?)del
GRCh38.p12First PassNC_000006.12Chr6160,207,873160,217,044
essv5003951RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5006575RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5007617RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5015342RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5019869RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5025963RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5027323RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5030128RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5030774RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5032578RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5036758RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5038118RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5039685RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5041347RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5048344RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5060706RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5061230RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5063343RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5068365RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5087087RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5089183RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5091877RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5104273RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5111988RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5114788RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5123797RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5132067RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5133421RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5143871RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5144936RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5151512RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5155585RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5155910RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5158450RemappedPerfectNC_000006.11:g.(?_
160628905)_(160638
076_?)del
GRCh37.p13First PassNC_000006.11Chr6160,628,905160,638,076
essv5003951Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5006575Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5007617Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5015342Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5019869Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5025963Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5027323Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5030128Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5030774Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5032578Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5036758Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5038118Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5039685Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5041347Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5048344Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5060706Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5061230Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5063343Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5068365Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5087087Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5089183Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5091877Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5104273Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5111988Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5114788Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5123797Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5132067Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5133421Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5143871Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5144936Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5151512Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
essv5155585Submitted genomicNC_000006.10:g.(?_
160548895)_(160558
066_?)del
NCBI36 (hg18)NC_000006.10Chr6160,548,895160,558,066
Showing 100 of 102

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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