A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5822859



Internal ID8800262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29798436..29954897hg38UCSC Ensembl
chr6:29766213..29922674hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38156462
hg19156462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674862
Supporting Variants
SamplesNA18959
Known GenesHCG4B, HLA-A, HLA-G, HLA-H
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5822859
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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