A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686877



Internal ID15423529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37423192..37423443hg38UCSC Ensembl
Innerchr20:36051595..36051846hg19UCSC Ensembl
Innerchr20:35485009..35485260hg18UCSC Ensembl
Innerchr20:35485009..35485260hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38252
hg19252
hg18252
hg17252
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516343
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686877
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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