A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869858



Internal ID15817128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36107306..36192375hg38UCSC Ensembl
Innerchr17:34434699..34519762hg19UCSC Ensembl
Innerchr17:31458812..31543875hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3885070
hg1985064
hg1885064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574759
Supporting Variants
Samples
Known GenesTBC1D3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869858
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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