A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668848



Internal ID9934953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168732602..168735825hg38UCSC Ensembl
Outerchr6:168732445..168735978hg38UCSC Ensembl
Innerchr6:169132678..169135907hg19UCSC Ensembl
Outerchr6:169132521..169136060hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383534
hg193540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5743397
SamplesNA19070
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668848
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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