A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659673



Internal ID9925778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20569222..20576050hg38UCSC Ensembl
Outerchr2:20569065..20576203hg38UCSC Ensembl
Innerchr2:20768982..20775810hg19UCSC Ensembl
Outerchr2:20768825..20775963hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg387139
hg197139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5439960
SamplesNA18538
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659673
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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