A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742694



Internal ID18716940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:103370671..103370923hg38UCSC Ensembl
Outerchr8:103370604..103370994hg38UCSC Ensembl
Innerchr8:104382899..104383151hg19UCSC Ensembl
Outerchr8:104382832..104383222hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543947
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742694
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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