A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701737



Internal ID15438389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59497591..59501402hg38UCSC Ensembl
Innerchr20:58072646..58076457hg19UCSC Ensembl
Innerchr20:57506041..57509852hg18UCSC Ensembl
Innerchr20:57506041..57509852hg17UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg383812
hg193812
hg183812
hg173812
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525595
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701737
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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