A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567042



Internal ID18768118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:174180110..174180392hg38UCSC Ensembl
Outerchr5:174180050..174180445hg38UCSC Ensembl
Innerchr5:173607113..173607395hg19UCSC Ensembl
Outerchr5:173607053..173607448hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765789
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567042
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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