A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517179



Internal ID15444472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:87817327..87836921hg38UCSC Ensembl
Innerchr1:88283010..88302604hg19UCSC Ensembl
Innerchr1:88055598..88075192hg18UCSC Ensembl
Innerchr1:87995031..88014625hg17UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3819595
hg1919595
hg1819595
hg1719595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653937, nssv661396
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517179
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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