A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591559



Internal ID6631843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86764344..86832450hg38UCSC Ensembl
chr2:86991467..87059573hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3868107
hg1968107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10571514
SamplesNA12287
Known GenesCD8A, CD8B, RMND5A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591559
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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