A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742650



Internal ID18716896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97583185..97583500hg38UCSC Ensembl
Outerchr8:97583116..97583544hg38UCSC Ensembl
Innerchr8:98595413..98595728hg19UCSC Ensembl
Outerchr8:98595344..98595772hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742650
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer