A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589958



Internal ID6977286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18142097..18163586hg38UCSC Ensembl
chr2:18323363..18344852hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3821490
hg1921490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10421743, essv10421742, essv10421741
SamplesHG00109, HG00130, NA19707
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589958
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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