A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665380



Internal ID9931485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32554639..32595345hg38UCSC Ensembl
Outerchr6:32554268..32595715hg38UCSC Ensembl
Innerchr6:32522416..32563122hg19UCSC Ensembl
Outerchr6:32522045..32563492hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3841448
hg1941448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1106e199
Supporting Variantsessv6532860, essv6068400, essv5815847, essv5853586, essv6198856
SamplesHG01521, HG01518, HG01522, HG01519, HG01516
Known GenesHLA-DRB1, HLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665380
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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