A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595614



Internal ID6982932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25843790..25851069hg38UCSC Ensembl
chr3:25885281..25892560hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg387280
hg197280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10954232
SamplesHG02589
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595614
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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