A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662380



Internal ID15399032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24429559..24440534hg38UCSC Ensembl
Innerchr20:24410195..24421170hg19UCSC Ensembl
Innerchr20:24358195..24369170hg18UCSC Ensembl
Innerchr20:24358195..24369170hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3810976
hg1910976
hg1810976
hg1710976
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515713
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662380
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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