A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665861



Internal ID9931966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:67044149..67104147hg38UCSC Ensembl
Outerchr2:67044112..67104197hg38UCSC Ensembl
Innerchr2:67271281..67331279hg19UCSC Ensembl
Outerchr2:67271244..67331329hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3860086
hg1960086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6574764
SamplesNA18989
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665861
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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