A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523329



Internal ID15450622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100357200..100383774hg38UCSC Ensembl
Innerchr13:101009454..101036028hg19UCSC Ensembl
Innerchr13:99807455..99834029hg18UCSC Ensembl
Innerchr13:99807455..99834029hg17UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3826575
hg1926575
hg1826575
hg1726575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699073
Samples
Known GenesPCCA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523329
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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