A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6598258



Internal ID9368209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32486627..32546399hg38UCSC Ensembl
Outerchr6:32486593..32546434hg38UCSC Ensembl
Innerchr6:32454404..32514176hg19UCSC Ensembl
Outerchr6:32454370..32514211hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3859842
hg1959842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658893
Supporting Variants
SamplesNA18561
Known GenesHLA-DRB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6598258
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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