A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702146



Internal ID15092112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5922677..5923394hg38UCSC Ensembl
Innerchr20:5903323..5904040hg19UCSC Ensembl
Innerchr20:5851323..5852040hg18UCSC Ensembl
Innerchr20:5851323..5852040hg17UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38718
hg19718
hg18718
hg17718
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525940
Supporting Variants
Samples
Known GenesCHGB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702146
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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