A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv986952



Internal ID16280908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196334962..196337052hg38UCSC Ensembl
Innerchr3:196061833..196063923hg19UCSC Ensembl
Innerchr3:197546230..197548320hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382091
hg192091
hg182091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593085
Supporting Variants
Samples
Known GenesTM4SF19, TM4SF19-TCTEX1D2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv986952
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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