A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662021



Internal ID15398673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16580558..16604669hg38UCSC Ensembl
Innerchr20:16561203..16585314hg19UCSC Ensembl
Innerchr20:16509203..16533314hg18UCSC Ensembl
Innerchr20:16509203..16533314hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3824112
hg1924112
hg1824112
hg1724112
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517032
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662021
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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