A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3543975



Internal ID18745051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:107108014..107108259hg38UCSC Ensembl
Outerchr8:107107963..107108326hg38UCSC Ensembl
Innerchr8:108120242..108120487hg19UCSC Ensembl
Outerchr8:108120191..108120554hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9742722
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3543975
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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