A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528336



Internal ID15455629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:29620151..29652361hg38UCSC Ensembl
Innerchr13:30194288..30226498hg19UCSC Ensembl
Innerchr13:29092288..29124498hg18UCSC Ensembl
Innerchr13:29092288..29124498hg17UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3832211
hg1932211
hg1832211
hg1732211
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704918
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528336
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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