A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523733



Internal ID15451026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84266446..84272997hg38UCSC Ensembl
Innerchr10:86026202..86032753hg19UCSC Ensembl
Innerchr10:86016182..86022733hg18UCSC Ensembl
Innerchr10:86016182..86022733hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg386552
hg196552
hg186552
hg176552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699549
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523733
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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