A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671253



Internal ID9590672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29912030..29997020hg38UCSC Ensembl
Outerchr6:29911996..29997055hg38UCSC Ensembl
Innerchr6:29879807..29964797hg19UCSC Ensembl
Outerchr6:29879773..29964832hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3885060
hg1985060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1088e199
Supporting Variantsessv5730981
SamplesHG00127
Known GenesHCG4B, HCG9, HLA-A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671253
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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