A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676943



Internal ID9943048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107260085..107263429hg38UCSC Ensembl
Outerchr6:107259928..107263582hg38UCSC Ensembl
Innerchr6:107581289..107584633hg19UCSC Ensembl
Outerchr6:107581132..107584786hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383655
hg193655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6209662
SamplesNA19079
Known GenesPDSS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676943
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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