A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589627



Internal ID6976956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1374509..1408170hg38UCSC Ensembl
chr2:1378281..1411942hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3833662
hg1933662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10386723
SamplesNA19078
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589627
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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