A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6425891



Internal ID9403294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32551508..32577533hg38UCSC Ensembl
Outerchr6:32551474..32577568hg38UCSC Ensembl
Innerchr6:32519285..32545310hg19UCSC Ensembl
Outerchr6:32519251..32545345hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826095
hg1926095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656607
Supporting Variants
SamplesNA19003
Known GenesHLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6425891
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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