A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660890



Internal ID9580309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32554611..32581450hg38UCSC Ensembl
Outerchr6:32554568..32581495hg38UCSC Ensembl
Innerchr6:32522388..32549227hg19UCSC Ensembl
Outerchr6:32522345..32549272hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826928
hg1926928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1108e199
Supporting Variantsessv5592026, essv5816507, essv5402778, essv5885966, essv6191050
SamplesHG00689, HG00326, NA18559, HG00252, HG00472
Known GenesHLA-DRB1, HLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660890
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer