A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667884



Internal ID9933989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31274732..31359727hg38UCSC Ensembl
chr6:31242509..31327504hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3884996
hg1984996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1094e199
Supporting Variantsessv5711337, essv6122450
SamplesHG00142, HG01149
Known GenesHLA-B, MIR6891
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667884
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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