A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015894



Internal ID19105112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32481273..32549139hg38UCSC Ensembl
Innerchr6:32449050..32516916hg19UCSC Ensembl
Innerchr6:32557028..32624894hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3867867
hg1967867
hg1867867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5948n100
Supporting Variantsnssv3655961
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015894
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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