A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527396



Internal ID15454689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:55804148..55815236hg38UCSC Ensembl
Innerchr1:56269821..56280909hg19UCSC Ensembl
Innerchr1:56042409..56053497hg18UCSC Ensembl
Innerchr1:55981842..55992930hg17UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3811089
hg1911089
hg1811089
hg1711089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703831
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527396
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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