A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755159



Internal ID18382719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41552949..41555766hg38UCSC Ensembl
Outerchr19:41552653..41555772hg38UCSC Ensembl
Innerchr19:42059319..42062136hg19UCSC Ensembl
Outerchr19:42059023..42062142hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383120
hg193120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556412
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755159
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