A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657463



Internal ID9923568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27404242..27405312hg38UCSC Ensembl
Outerchr6:27404085..27405465hg38UCSC Ensembl
Innerchr6:27372021..27373091hg19UCSC Ensembl
Outerchr6:27371864..27373244hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381381
hg191381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6178086
SamplesHG00237
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657463
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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