A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526157



Internal ID15453450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63702033..63719655hg38UCSC Ensembl
Innerchr10:65461793..65479415hg19UCSC Ensembl
Innerchr10:65131799..65149421hg18UCSC Ensembl
Innerchr10:65131799..65149421hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3817623
hg1917623
hg1817623
hg1717623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702416
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526157
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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