A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619769



Internal ID7006643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15166239..15337990hg38UCSC Ensembl
chr9:15166237..15337988hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38171752
hg19171752
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13408015, essv13408012, essv13408014, essv13408016, essv13408013
SamplesNA21127, HG03039, HG03097, HG03060, HG03077
Known GenesTTC39B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619769
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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