A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016516



Internal ID19105735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120687722..120797095hg38UCSC Ensembl
Innerchr5:120023417..120132790hg19UCSC Ensembl
Innerchr5:120051316..120160689hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38109374
hg19109374
hg18109374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5797n100
Supporting Variantsnssv3647985
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016516
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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