A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699111



Internal ID15435763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:18400131..18433712hg38UCSC Ensembl
Innerchr20:18380775..18414356hg19UCSC Ensembl
Innerchr20:18328775..18362356hg18UCSC Ensembl
Innerchr20:18328775..18362356hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3833582
hg1933582
hg1833582
hg1733582
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523362
Supporting Variants
Samples
Known GenesDZANK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699111
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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