A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv651968



Internal ID15388620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45727555..45749938hg38UCSC Ensembl
Innerchr20:44356194..44378577hg19UCSC Ensembl
Innerchr20:43789608..43811984hg18UCSC Ensembl
Innerchr20:43789608..43811984hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3822384
hg1922384
hg1822377
hg1722377
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517420
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv651968
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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