A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760313



Internal ID16054269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122143256..122166795hg38UCSC Ensembl
Innerchr10:123902771..123926310hg19UCSC Ensembl
Innerchr10:123892761..123916300hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3823540
hg1923540
hg1823540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552246
Supporting Variants
Samples
Known GenesTACC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv760313
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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