A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619763



Internal ID7006637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15140390..15207671hg38UCSC Ensembl
chr9:15140388..15207669hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3867282
hg1967282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13407862, essv13407863, essv13407864, essv13407865
SamplesHG03039, HG03097, HG03060, HG03077
Known GenesTTC39B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619763
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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