A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523067



Internal ID15450360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83481311..83488145hg38UCSC Ensembl
Innerchr13:84055446..84062280hg19UCSC Ensembl
Innerchr13:82953447..82960281hg18UCSC Ensembl
Innerchr13:82953447..82960281hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg386835
hg196835
hg186835
hg176835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698753
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523067
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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