A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619045



Internal ID6659238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140953452..140965524hg38UCSC Ensembl
chr8:141963551..141975623hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3812073
hg1912073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1425e214
Supporting Variantsessv13358314
SamplesHG03069
Known GenesPTK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619045
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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