A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686414



Internal ID15423066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20561695..20573498hg38UCSC Ensembl
Innerchr10:20850624..20862427hg19UCSC Ensembl
Innerchr10:20890630..20902433hg18UCSC Ensembl
Innerchr10:20890630..20902433hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3811804
hg1911804
hg1811804
hg1711804
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516763
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686414
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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