A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742306



Internal ID18716552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60292460..60292735hg38UCSC Ensembl
Outerchr8:60292394..60292785hg38UCSC Ensembl
Innerchr8:61205019..61205294hg19UCSC Ensembl
Outerchr8:61204953..61205344hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742306
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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