A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024742



Internal ID19113959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32655500..32702718hg38UCSC Ensembl
Innerchr6:32623277..32670495hg19UCSC Ensembl
Innerchr6:32731255..32778473hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3847219
hg1947219
hg1847219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5951n100
Supporting Variantsnssv3657339
Samples
Known GenesHLA-DQB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024742
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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