A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520219



Internal ID15447512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127835444..127843238hg38UCSC Ensembl
Innerchr10:129633708..129641502hg19UCSC Ensembl
Innerchr10:129523698..129531492hg18UCSC Ensembl
Innerchr10:129523698..129531492hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg387795
hg197795
hg187795
hg177795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697289
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520219
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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