A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563142



Internal ID18764218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195023369..195023577hg38UCSC Ensembl
Outerchr3:195023321..195023597hg38UCSC Ensembl
Innerchr3:194744098..194744306hg19UCSC Ensembl
Outerchr3:194744050..194744326hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761889
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563142
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