A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519044



Internal ID15446337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65172050..65224171hg38UCSC Ensembl
Innerchr13:65746182..65798303hg19UCSC Ensembl
Innerchr13:64644183..64696304hg18UCSC Ensembl
Innerchr13:64644183..64696304hg17UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3852122
hg1952122
hg1852122
hg1752122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696514
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519044
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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