A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619766



Internal ID7006640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15163388..15206006hg38UCSC Ensembl
chr9:15163386..15206004hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3842619
hg1942619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13408009, essv13408008, essv13408007, essv13408006
SamplesHG03039, HG03097, HG03060, HG03077
Known GenesTTC39B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619766
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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