A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659406



Internal ID9925512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46189072..46195005hg38UCSC Ensembl
chr2:46416211..46422144hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg385934
hg195934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5843327, essv6554998
SamplesNA19446, NA19398
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659406
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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