A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667424



Internal ID9586843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:132912075..132916871hg38UCSC Ensembl
Outerchr2:132912041..132916906hg38UCSC Ensembl
Innerchr2:133669648..133674444hg19UCSC Ensembl
Outerchr2:133669614..133674479hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg384866
hg194866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv733e199
Supporting Variantsessv6523259
SamplesHG00182
Known GenesMIR7853, NCKAP5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667424
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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