A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5950n100



Internal ID22792037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32485140..32589524hg38UCSC Ensembl
chr6:32452917..32557301hg19UCSC Ensembl
chr6:32560895..32665279hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38104385
hg19104385
hg18104385
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028445, nsv1027396
Samples
Known GenesHLA-DRB1, 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)dgv5950n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss2
Observed Complex0
Frequencyn/a


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