A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749906



Internal ID16043862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66569424..66826267hg38UCSC Ensembl
Innerchr10:68329182..68586025hg19UCSC Ensembl
Innerchr10:67999188..68256031hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38256844
hg19256844
hg18256844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551382
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)nssv749906
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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