A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv746838



Internal ID15694108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34931247..35060646hg38UCSC Ensembl
Innerchr10:35220175..35349574hg19UCSC Ensembl
Innerchr10:35260181..35389580hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38129400
hg19129400
hg18129400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550401
Supporting Variants
Samples
Known GenesCUL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv746838
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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