A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1094e199



Internal ID22758867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31267135..31362669hg38UCSC Ensembl
chr6:31234912..31330446hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3895535
hg1995535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2675568, esv2667884, esv2671491, esv2656634, esv2666002, esv2678423, esv2668514
SamplesHG00142, NA18528, NA20507, NA12341, NA20755, NA18933, HG01149, NA19117, NA19474
Known GenesHLA-B, HLA-C, MIR6891
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1094e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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