A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526052



Internal ID15453345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:33659067..33721862hg38UCSC Ensembl
Innerchr10:33947995..34010790hg19UCSC Ensembl
Innerchr10:33988001..34050796hg18UCSC Ensembl
Innerchr10:33988001..34050796hg17UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3862796
hg1962796
hg1862796
hg1762796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702289
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526052
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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