A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694723



Internal ID15431375
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521954
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694723
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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