A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703791



Internal ID15440443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54919913..54931733hg38UCSC Ensembl
Innerchr1:55385586..55397406hg19UCSC Ensembl
Innerchr1:55158174..55169994hg18UCSC Ensembl
Innerchr1:55097607..55109427hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3811821
hg1911821
hg1811821
hg1711821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527361
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703791
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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