A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678651



Internal ID9944756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:81418212..81426704hg38UCSC Ensembl
Outerchr6:81418175..81426754hg38UCSC Ensembl
Innerchr6:82127929..82136421hg19UCSC Ensembl
Outerchr6:82127892..82136471hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg388580
hg198580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6020126
SamplesNA19116
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678651
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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