U.S. flag

An official website of the United States government

esv2421962

  • Variant Calls:39
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,251

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 226 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):42,351,574-42,357,824Question Mark
Overlapping variant regions from other studies: 226 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):39,931,539-39,937,789Question Mark
Overlapping variant regions from other studies: 81 SVs from 11 studies. See in: genome view    
Submitted genomic38,185,537-38,191,787Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2421962RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1842,351,57442,357,824
esv2421962RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1839,931,53939,937,789
esv2421962Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000018.8Chr1838,185,53738,191,787

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
essv5011345deletionNA21723SNP arraySNP genotyping analysis1138
essv5015916deletionNA18861SNP arraySNP genotyping analysis1137
essv5018470deletionNA21418SNP arraySNP genotyping analysis1141
essv5026174deletionNA19210SNP arraySNP genotyping analysis1149
essv5027851deletionNA19102SNP arraySNP genotyping analysis1141
essv5032128deletionNA19174SNP arraySNP genotyping analysis1142
essv5032744deletionNA19679SNP arraySNP genotyping analysis1125
essv5036079deletionNA18869SNP arraySNP genotyping analysis1140
essv5037372deletionNA19118SNP arraySNP genotyping analysis1127
essv5037415deletionNA19226SNP arraySNP genotyping analysis1156
essv5037940deletionNA21339SNP arraySNP genotyping analysis1143
essv5046115deletionNA21685SNP arraySNP genotyping analysis1153
essv5049552deletionNA19248SNP arraySNP genotyping analysis1145
essv5049603deletionNA21489SNP arraySNP genotyping analysis1131
essv5051861deletionNA18871SNP arraySNP genotyping analysis1151
essv5053296deletionNA19103SNP arraySNP genotyping analysis1143
essv5068262deletionNA20348SNP arraySNP genotyping analysis1167
essv5071232deletionNA18911SNP arraySNP genotyping analysis1158
essv5071502deletionNA21636SNP arraySNP genotyping analysis1134
essv5077447deletionNA21634SNP arraySNP genotyping analysis1128
essv5086707deletionNA21451SNP arraySNP genotyping analysis1137
essv5093282deletionNA20277SNP arraySNP genotyping analysis1135
essv5096853deletionNA11894SNP arraySNP genotyping analysis1122
essv5102942deletionNA18484SNP arraySNP genotyping analysis1143
essv5114140deletionNA18863SNP arraySNP genotyping analysis1149
essv5123578deletionNA18910SNP arraySNP genotyping analysis1154
essv5124037deletionNA18486SNP arraySNP genotyping analysis1158
essv5127347deletionNA19096SNP arraySNP genotyping analysis1138
essv5129129deletionNA19176SNP arraySNP genotyping analysis1162
essv5129391deletionNA19097SNP arraySNP genotyping analysis1146
essv5131200deletionNA21365SNP arraySNP genotyping analysis1129
essv5134428deletionNA21575SNP arraySNP genotyping analysis1136
essv5140814deletionNA19440SNP arraySNP genotyping analysis1131
essv5141713deletionNA18868SNP arraySNP genotyping analysis1148
essv5145552deletionNA19982SNP arraySNP genotyping analysis1139
essv5147349deletionNA21617SNP arraySNP genotyping analysis1155
essv5158028deletionNA21366SNP arraySNP genotyping analysis1137
essv5158520deletionNA19373SNP arraySNP genotyping analysis1138
essv5159923deletionNA19651SNP arraySNP genotyping analysis1156

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5011345RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5015916RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5018470RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5026174RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5027851RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5032128RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5032744RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5036079RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5037372RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5037415RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5037940RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5046115RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5049552RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5049603RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5051861RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5053296RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5068262RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5071232RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5071502RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5077447RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5086707RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5093282RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5096853RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5102942RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5114140RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5123578RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5124037RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5127347RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5129129RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5129391RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5131200RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5134428RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5140814RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5141713RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5145552RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5147349RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5158028RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5158520RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5159923RemappedPerfectNC_000018.10:g.(?_
42351574)_(4235782
4_?)del
GRCh38.p12First PassNC_000018.10Chr1842,351,57442,357,824
essv5011345RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5015916RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5018470RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5026174RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5027851RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5032128RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5032744RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5036079RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5037372RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5037415RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5037940RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5046115RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5049552RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5049603RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5051861RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5053296RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5068262RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5071232RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5071502RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5077447RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5086707RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5093282RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5096853RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5102942RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5114140RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5123578RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5124037RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5127347RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5129129RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5129391RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5131200RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5134428RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5140814RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5141713RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5145552RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5147349RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5158028RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5158520RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5159923RemappedPerfectNC_000018.9:g.(?_3
9931539)_(39937789
_?)del
GRCh37.p13First PassNC_000018.9Chr1839,931,53939,937,789
essv5011345Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5015916Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5018470Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5026174Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5027851Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5032128Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5032744Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5036079Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5037372Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5037415Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5037940Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5046115Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5049552Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5049603Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5051861Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5053296Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5068262Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5071232Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5071502Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5077447Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5086707Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
essv5093282Submitted genomicNC_000018.8:g.(?_3
8185537)_(38191787
_?)del
NCBI36 (hg18)NC_000018.8Chr1838,185,53738,191,787
Showing 100 of 117

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

Support Center