A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596976



Internal ID6984290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89806027..89891703hg38UCSC Ensembl
chr3:89855177..89940853hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3885677
hg1985677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11069202, essv11069203, essv11069204
SamplesHG03926, HG02882, NA12716
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596976
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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