A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589903



Internal ID6977233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15016319..15057663hg38UCSC Ensembl
Innerchr2:15016469..15057513hg38UCSC Ensembl
Outerchr2:15016169..15057813hg38UCSC Ensembl
chr2:15156443..15197787hg19UCSC Ensembl
Innerchr2:15156593..15197637hg19UCSC Ensembl
Outerchr2:15156293..15197937hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3841345
hg1941345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10415060, essv10415059, essv10415058, essv10415057, essv10415056
SamplesHG01853, HG01997, HG03160, HG01598, NA18615
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589903
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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