A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755064



Internal ID18729310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34236773..34239463hg38UCSC Ensembl
Outerchr19:34236620..34239745hg38UCSC Ensembl
Innerchr19:34727678..34730368hg19UCSC Ensembl
Outerchr19:34727525..34730650hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383126
hg193126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556317
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755064
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