A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1093e199



Internal ID11593352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31240921..31345116hg38UCSC Ensembl
chr6:31208698..31312893hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38104196
hg19104196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2659670, esv2674481
SamplesNA19725, NA18564
Known GenesHLA-C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1093e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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