A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1113e199



Internal ID6312217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32629709..32728580hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsesv2657468, esv2658200, esv2673271
SamplesHG01055, HG01134, NA18559, NA18637, HG00133, NA18597, HG00119
Known GenesHLA-DQA2, HLA-DQB1, HLA-DQB2
Method
Analysis
Platform
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1113e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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