A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589629



Internal ID6629918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1422992..1482602hg38UCSC Ensembl
chr2:1426764..1486374hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3859611
hg1959611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10386729, essv10386728, essv10386727, essv10386726
SamplesHG03577, NA18856, NA19078, HG03303
Known GenesTPO
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589629
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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