A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997893



Internal ID19157429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195774521..195915321hg38UCSC Ensembl
Innerchr3:195501392..195642192hg19UCSC Ensembl
Innerchr3:196987026..197126589hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38140801
hg19140801
hg18139564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5034n100
Supporting Variantsnssv3616983
Samples
Known GenesMIR6829, MUC4, TNK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997893
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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