A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523666



Internal ID15450959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39655754..39656157hg38UCSC Ensembl
Innerchr13:40229891..40230294hg19UCSC Ensembl
Innerchr13:39127891..39128294hg18UCSC Ensembl
Innerchr13:39127891..39128294hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38404
hg19404
hg18404
hg17404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699468
Samples
Known GenesCOG6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523666
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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