A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689371



Internal ID15426023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20561695..20565639hg38UCSC Ensembl
Innerchr10:20850624..20854568hg19UCSC Ensembl
Innerchr10:20890630..20894574hg18UCSC Ensembl
Innerchr10:20890630..20894574hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg383945
hg193945
hg183945
hg173945
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)nssv689371
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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