A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676073



Internal ID9942178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32516152..32577818hg38UCSC Ensembl
Outerchr6:32516118..32577853hg38UCSC Ensembl
Innerchr6:32483929..32545595hg19UCSC Ensembl
Outerchr6:32483895..32545630hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3861736
hg1961736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1105e199
Supporting Variantsessv5424830
SamplesHG01259
Known GenesHLA-DRB5, HLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676073
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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