A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6161153



Internal ID9301027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33125630..33125961hg38UCSC Ensembl
chr6:33093407..33093738hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676552
Supporting Variants
SamplesNA12892
Known GenesHLA-DPB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6161153
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer