A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661853



Internal ID9927958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:225825533..225849286hg38UCSC Ensembl
Outerchr2:225825496..225849336hg38UCSC Ensembl
Innerchr2:226690249..226714002hg19UCSC Ensembl
Outerchr2:226690212..226714052hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3823841
hg1923841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6039538
SamplesNA18611
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661853
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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