A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695440



Internal ID15432092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81119963..81181999hg38UCSC Ensembl
Innerchr10:82879719..82941755hg19UCSC Ensembl
Innerchr10:82869699..82931735hg18UCSC Ensembl
Innerchr10:82869699..82931735hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3862037
hg1962037
hg1862037
hg1762037
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518030
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695440
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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