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nsv471691

  • Variant Calls:19
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:205,688

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 995 SVs from 104 studies. See in: genome view    
Remapped(Score: Perfect):22,469,014-22,674,701Question Mark
Overlapping variant regions from other studies: 995 SVs from 104 studies. See in: genome view    
Remapped(Score: Perfect):22,480,335-22,686,022Question Mark
Overlapping variant regions from other studies: 2 SVs from 2 studies. See in: genome view    
Submitted genomic22,446,888-22,652,575Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv471691RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1622,469,01422,674,701
nsv471691RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1622,480,33522,686,022
nsv471691Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000016.7Chr1622,446,88822,652,575

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv551139copy number gainGM10469ABAC aCGHProbe signal intensity56
nssv551140copy number gainGM10470ABAC aCGHProbe signal intensity49
nssv551141copy number gainGM10471BAC aCGHProbe signal intensity51
nssv551142copy number gainGM10492ABAC aCGHProbe signal intensity47
nssv551143copy number gainGM10493BAC aCGHProbe signal intensity65
nssv551144copy number gainGM10494ABAC aCGHProbe signal intensity55
nssv551145copy number gainGM10495BBAC aCGHProbe signal intensity45
nssv551146copy number gainGM10971BAC aCGHProbe signal intensity56
nssv551147copy number gainGM11323BAC aCGHProbe signal intensity53
nssv551148copy number gainGM11521BAC aCGHProbe signal intensity49
nssv551149copy number gainGM17014ABAC aCGHProbe signal intensity61
nssv551150copy number gainGM17017BAC aCGHProbe signal intensity57
nssv551151copy number lossGM17052BAC aCGHProbe signal intensity50
nssv551152copy number gainJK1051ABAC aCGHProbe signal intensity53
nssv551153copy number gainJK1058BBAC aCGHProbe signal intensity61
nssv551154copy number gainJK1061BAC aCGHProbe signal intensity51
nssv551155copy number gainJK1688BBAC aCGHProbe signal intensity53
nssv551156copy number gainJK776BAC aCGHProbe signal intensity50
nssv551157copy number gainP86GABAC aCGHProbe signal intensity50

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv551139RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551140RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551141RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551142RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551143RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551144RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551145RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551146RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551147RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551148RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551149RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551150RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551151RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)del
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551152RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551153RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551154RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551155RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551156RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551157RemappedPerfectNC_000016.10:g.(?_
22469014)_(2267470
1_?)dup
GRCh38.p12First PassNC_000016.10Chr1622,469,01422,674,701
nssv551139RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551140RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551141RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551142RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551143RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551144RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551145RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551146RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551147RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551148RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551149RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551150RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551151RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)del
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551152RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551153RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551154RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551155RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551156RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551157RemappedPerfectNC_000016.9:g.(?_2
2480335)_(22686022
_?)dup
GRCh37.p13First PassNC_000016.9Chr1622,480,33522,686,022
nssv551139Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551140Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551141Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551142Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551143Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551144Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551145Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551146Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551147Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551148Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551149Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551150Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551151Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)del
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551152Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551153Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551154Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551155Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551156Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575
nssv551157Submitted genomicNC_000016.7:g.(?_2
2446888)_(22652575
_?)dup
NCBI34 (hg16)NC_000016.7Chr1622,446,88822,652,575

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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