A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742482



Internal ID18716728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:81132871..81134349hg38UCSC Ensembl
Outerchr8:81132588..81134459hg38UCSC Ensembl
Innerchr8:82045106..82046584hg19UCSC Ensembl
Outerchr8:82044823..82046694hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381872
hg191872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543735
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742482
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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