A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658963



Internal ID15395615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126892746..126896428hg38UCSC Ensembl
Innerchr10:128581315..128584997hg19UCSC Ensembl
Innerchr10:128571305..128574987hg18UCSC Ensembl
Innerchr10:128571305..128574987hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383683
hg193683
hg183683
hg173683
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515706
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658963
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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