A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6492161



Internal ID9084015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32624839..32665445hg38UCSC Ensembl
Outerchr6:32624468..32665815hg38UCSC Ensembl
Innerchr6:32592616..32633222hg19UCSC Ensembl
Outerchr6:32592245..32633592hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3841348
hg1941348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676495
Supporting Variants
SamplesHG01061
Known GenesHLA-DQA1, HLA-DQB1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6492161
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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