A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5842253



Internal ID8865602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32550539..32573745hg38UCSC Ensembl
Outerchr6:32550168..32574115hg38UCSC Ensembl
Innerchr6:32518316..32541522hg19UCSC Ensembl
Outerchr6:32517945..32541892hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3823948
hg1923948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673467
Supporting Variants
SamplesHG00320
Known GenesHLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5842253
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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