A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596869



Internal ID6984183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86650507..86749226hg38UCSC Ensembl
chr3:86699657..86798376hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3898720
hg1998720
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11063815
SamplesNA20287
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596869
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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