A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1113e199



Internal ID11593372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32661932..32760803hg38UCSC Ensembl
chr6:32629709..32728580hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3898872
hg1998872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2657468, esv2658200, esv2673271
SamplesHG01055, HG01134, NA18559, NA18637, HG00133, NA18597, HG00119
Known GenesHLA-DQA2, HLA-DQB1, HLA-DQB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
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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