A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682279



Internal ID15418931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4971319..4991650hg38UCSC Ensembl
Innerchr1:5031379..5051710hg19UCSC Ensembl
Innerchr1:4931239..4951570hg18UCSC Ensembl
Innerchr1:4941752..4962083hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3820332
hg1920332
hg1820332
hg1720332
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521101
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682279
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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