A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619021



Internal ID7005902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139954391..139967986hg38UCSC Ensembl
Innerchr8:139954435..139967943hg38UCSC Ensembl
Outerchr8:139954348..139968030hg38UCSC Ensembl
chr8:140966689..140978191hg19UCSC Ensembl
Innerchr8:140966733..140978148hg19UCSC Ensembl
Outerchr8:140966646..140978235hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3813596
hg1911503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13351961, essv13351960
SamplesNA18960, HG00182
Known GenesTRAPPC9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619021
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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