A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653997



Internal ID15390649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:40426392..40438275hg38UCSC Ensembl
Innerchr20:39055032..39066915hg19UCSC Ensembl
Innerchr20:38488446..38500329hg18UCSC Ensembl
Innerchr20:38488446..38500329hg17UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3811884
hg1911884
hg1811884
hg1711884
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517474
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653997
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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