A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596876



Internal ID6984190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86831686..86836866hg38UCSC Ensembl
chr3:86880836..86886016hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg385181
hg195181
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11063940, essv11063935, essv11063938, essv11063937, essv11063939, essv11063936
SamplesHG03941, HG01171, HG00282, HG00263, HG00099, HG02684
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596876
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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