A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676274



Internal ID9942379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153931370..153931962hg38UCSC Ensembl
Outerchr6:153931333..153932012hg38UCSC Ensembl
Innerchr6:154252505..154253097hg19UCSC Ensembl
Outerchr6:154252468..154253147hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5728193
SamplesNA18517
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676274
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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