A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5699135



Internal ID8676538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29798766..29955223hg38UCSC Ensembl
chr6:29766543..29923000hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38156458
hg19156458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671225
Supporting Variants
SamplesNA19448
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)essv5699135
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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