A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673271



Internal ID9939376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32663942..32760768hg38UCSC Ensembl
Outerchr6:32663908..32760803hg38UCSC Ensembl
Innerchr6:32631719..32728545hg19UCSC Ensembl
Outerchr6:32631685..32728580hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3896896
hg1996896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1113e199
Supporting Variantsessv6136858
SamplesHG00133
Known GenesHLA-DQA2, HLA-DQB1, HLA-DQB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673271
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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