A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749901



Internal ID16043857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66557325..66799596hg38UCSC Ensembl
Innerchr10:68317083..68559354hg19UCSC Ensembl
Innerchr10:67987089..68229360hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38242272
hg19242272
hg18242272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551375
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)nssv749901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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