A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665843



Internal ID9931948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112702882..112727074hg38UCSC Ensembl
chr2:113460459..113484651hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3824193
hg1924193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6495538, essv6500578
SamplesNA18960, NA18964
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665843
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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