A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667812



Internal ID9933917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:142923084..142924601hg38UCSC Ensembl
Outerchr3:142923047..142924651hg38UCSC Ensembl
Innerchr3:142641926..142643443hg19UCSC Ensembl
Outerchr3:142641889..142643493hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381605
hg191605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5717133
SamplesNA19819
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667812
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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