A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596942



Internal ID6984256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89034270..89037367hg38UCSC Ensembl
Innerchr3:89034299..89037339hg38UCSC Ensembl
Outerchr3:89034242..89037396hg38UCSC Ensembl
chr3:89083420..89086517hg19UCSC Ensembl
Innerchr3:89083449..89086489hg19UCSC Ensembl
Outerchr3:89083392..89086546hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg383098
hg193098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11068075, essv11068074
SamplesNA19000, HG04014
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596942
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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