A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3590098



Internal ID6977426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25685101..25690760hg38UCSC Ensembl
chr2:25907970..25913629hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg385660
hg195660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10433157
SamplesHG01435
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3590098
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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