A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003062



Internal ID19092279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195746913..195903829hg38UCSC Ensembl
Innerchr3:195473784..195630700hg19UCSC Ensembl
Innerchr3:196959455..197115097hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38156917
hg19156917
hg18155643
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5034n100
Supporting Variantsnssv3616982
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)nsv1003062
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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