A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749960



Internal ID16043916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67279551..67284717hg38UCSC Ensembl
Innerchr10:69039309..69044475hg19UCSC Ensembl
Innerchr10:68709315..68714481hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg385167
hg195167
hg185167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551422
Supporting Variants
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv749960
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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