A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664221



Internal ID9930326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15016319..15057663hg38UCSC Ensembl
chr2:15156443..15197787hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3841345
hg1941345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6163058
SamplesNA18615
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664221
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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