A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668598



Internal ID9934703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:98670820..98694106hg38UCSC Ensembl
Outerchr6:98670783..98694156hg38UCSC Ensembl
Innerchr6:99118696..99141982hg19UCSC Ensembl
Outerchr6:99118659..99142032hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3823374
hg1923374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5656367
SamplesNA12144
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668598
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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