A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596413



Internal ID6983728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65058896..65078147hg38UCSC Ensembl
chr3:65044571..65063822hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3819252
hg1919252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11029510, essv11029509
SamplesNA21119, HG03774
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596413
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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