A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693367



Internal ID15430019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20553102..20565151hg38UCSC Ensembl
Innerchr10:20842031..20854080hg19UCSC Ensembl
Innerchr10:20882037..20894086hg18UCSC Ensembl
Innerchr10:20882037..20894086hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3812050
hg1912050
hg1812050
hg1712050
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)nssv693367
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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