A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667584



Internal ID9933689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29890284..29945079hg38UCSC Ensembl
chr6:29858061..29912856hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854796
hg1954796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1087e199
Supporting Variantsessv6381187
SamplesNA18596
Known GenesHCG4B, HLA-A, HLA-H
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667584
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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