A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665698



Internal ID9585118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29828965..29943671hg38UCSC Ensembl
Outerchr6:29828931..29943706hg38UCSC Ensembl
Innerchr6:29796742..29911448hg19UCSC Ensembl
Outerchr6:29796708..29911483hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38114776
hg19114776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6176118
SamplesHG01140
Known GenesHCG4B, HLA-A, HLA-G, HLA-H
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665698
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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