A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5945n100



Internal ID19016313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32440750..32562509hg38UCSC Ensembl
chr6:32408527..32530286hg19UCSC Ensembl
chr6:32516505..32638264hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38121760
hg19121760
hg18121760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034950, nsv1025179
Samples
Known GenesHLA-DRA, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5945n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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