A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661098



Internal ID15397750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81119963..81126219hg38UCSC Ensembl
Innerchr10:82879719..82885975hg19UCSC Ensembl
Innerchr10:82869699..82875955hg18UCSC Ensembl
Innerchr10:82869699..82875955hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg386257
hg196257
hg186257
hg176257
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517526
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661098
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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