A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3543376



Internal ID18397766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38542228..38543094hg38UCSC Ensembl
Outerchr8:38542196..38543189hg38UCSC Ensembl
Innerchr8:38399746..38400612hg19UCSC Ensembl
Outerchr8:38399714..38400707hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9742123
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3543376
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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