A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662811



Internal ID9928916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:120848291..120853543hg38UCSC Ensembl
Outerchr3:120848134..120853696hg38UCSC Ensembl
Innerchr3:120567138..120572390hg19UCSC Ensembl
Outerchr3:120566981..120572543hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg385563
hg195563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5864768
SamplesNA20799
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662811
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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