A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959849



Internal ID16253805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:17339888..17497429hg38UCSC Ensembl
Innerchr3:17381380..17538921hg19UCSC Ensembl
Innerchr3:17356384..17513925hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38157542
hg19157542
hg18157542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589842
Supporting Variants
Samples
Known GenesTBC1D5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959849
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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