A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658200



Internal ID9924305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32661966..32758831hg38UCSC Ensembl
Outerchr6:32661932..32758866hg38UCSC Ensembl
Innerchr6:32629743..32726608hg19UCSC Ensembl
Outerchr6:32629709..32726643hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3896935
hg1996935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1113e199
Supporting Variantsessv6022592
SamplesNA18597
Known GenesHLA-DQA2, HLA-DQB1, HLA-DQB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658200
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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