A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596566



Internal ID6636836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74087246..74146685hg38UCSC Ensembl
chr3:74136397..74195836hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3859440
hg1959440
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11039399
SamplesHG03693
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596566
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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