A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616987



Internal ID18915268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195879899..195934667hg38UCSC Ensembl
Innerchr3:195606770..195661538hg19UCSC Ensembl
Innerchr3:197091167..197145935hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3854769
hg1954769
hg1854769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014602
Supporting Variants
Samples
Known GenesMIR6829, TNK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616987
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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