A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667151



Internal ID9586570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:218410438..218424824hg38UCSC Ensembl
Outerchr2:218410401..218424874hg38UCSC Ensembl
Innerchr2:219275161..219289547hg19UCSC Ensembl
Outerchr2:219275124..219289597hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3814474
hg1914474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6203730
SamplesNA18620
Known GenesVIL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667151
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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