A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760799



Internal ID16054755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130058387..130089848hg38UCSC Ensembl
Innerchr10:131856651..131888112hg19UCSC Ensembl
Innerchr10:131746641..131778102hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3831462
hg1931462
hg1831462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552317
Supporting Variants
Samples
Known GenesLINC00959
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv760799
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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