A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517795



Internal ID15445088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87184597..87241135hg38UCSC Ensembl
Innerchr13:87836852..87893390hg19UCSC Ensembl
Innerchr13:86634853..86691391hg18UCSC Ensembl
Innerchr13:86634853..86691391hg17UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3856539
hg1956539
hg1856539
hg1756539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694048
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517795
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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