A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521954



Internal ID15449247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:33723542..33725096hg38UCSC Ensembl
Innerchr13:34297679..34299233hg19UCSC Ensembl
Innerchr13:33195679..33197233hg18UCSC Ensembl
Innerchr13:33195679..33197233hg17UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg381555
hg191555
hg181555
hg171555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694723
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521954
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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