A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619034



Internal ID7005915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140403818..140438466hg38UCSC Ensembl
chr8:141413917..141448565hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3834649
hg1934649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13358281, essv13358282, essv13358283, essv13358280, essv13358279
SamplesNA19317, NA19026, NA19035, NA19017, NA19308
Known GenesTRAPPC9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619034
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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