A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520651



Internal ID15447944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132070850..132072825hg38UCSC Ensembl
Innerchr10:133884354..133886329hg19UCSC Ensembl
Innerchr10:133734344..133736319hg18UCSC Ensembl
Innerchr10:133734344..133736319hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381976
hg191976
hg181976
hg171976
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690233, nssv673554, nssv705914
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520651
Frequency
Sample Size2026
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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