A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152833



Internal ID15526396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143987719..144114635hg38UCSC Ensembl
Innerchr4:144908872..145035788hg19UCSC Ensembl
Innerchr4:145128322..145255238hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38126917
hg19126917
hg18126917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595611
Supporting Variants
SamplesHGDP00113
Known GenesGYPA, GYPB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152833
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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