A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1093e199



Internal ID6312197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31208698..31312893hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsesv2659670, esv2674481
SamplesNA19725, NA18564
Known GenesHLA-C
Method
Analysis
Platform
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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