A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3590964



Internal ID6978292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58575399..58992641hg38UCSC Ensembl
chr2:58802534..59219776hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38417243
hg19417243
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10517691
SamplesHG04186
Known GenesLINC01122
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3590964
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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