A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669311



Internal ID9935416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21049122..21052822hg38UCSC Ensembl
Outerchr2:21049085..21052872hg38UCSC Ensembl
Innerchr2:21271994..21275694hg19UCSC Ensembl
Outerchr2:21271957..21275744hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg383788
hg193788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6167003
SamplesNA20544
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669311
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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