A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518926



Internal ID15099533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33741162..33902088hg38UCSC Ensembl
Innerchr20:32328968..32489894hg19UCSC Ensembl
Innerchr20:31792629..31953555hg18UCSC Ensembl
Innerchr20:31792629..31953555hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38160927
hg19160927
hg18160927
hg17160927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696391
Samples
Known GenesCHMP4B, ZNF341
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518926
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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