A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523922



Internal ID15451215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:74663960..74664075hg38UCSC Ensembl
Innerchr13:75238097..75238212hg19UCSC Ensembl
Innerchr13:74136098..74136213hg18UCSC Ensembl
Innerchr13:74136098..74136213hg17UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38116
hg19116
hg18116
hg17116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699765
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523922
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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