A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664778



Internal ID9930883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32530191..32589693hg38UCSC Ensembl
Outerchr6:32530157..32589728hg38UCSC Ensembl
Innerchr6:32497968..32557470hg19UCSC Ensembl
Outerchr6:32497934..32557505hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3859572
hg1959572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1105e199
Supporting Variantsessv5469026
SamplesHG00372
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664778
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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