A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760688



Internal ID18734934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59139512..59139782hg38UCSC Ensembl
Outerchr3:59139481..59139851hg38UCSC Ensembl
Innerchr3:59125238..59125508hg19UCSC Ensembl
Outerchr3:59125207..59125577hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561941
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760688
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