A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574762



Internal ID16015485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36110820..36182044hg38UCSC Ensembl
Innerchr17:34438213..34509420hg19UCSC Ensembl
Innerchr17:31462326..31533533hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3871225
hg1971208
hg1871208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5536n54
Supporting Variantsnssv869862, nssv869863
Samples
Known GenesTBC1D3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574762
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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