A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515901



Internal ID15442958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125376500..125410838hg38UCSC Ensembl
Innerchr10:127065069..127099407hg19UCSC Ensembl
Innerchr10:127055059..127089397hg18UCSC Ensembl
Innerchr10:127055059..127089397hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3834339
hg1934339
hg1834339
hg1734339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706073, nssv665197, nssv680734
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515901
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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