A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755140



Internal ID18382700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40399855..40399905hg38UCSC Ensembl
chr19:40905762..40905812hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556393
Supporting Variants
Samples
Known GenesPRX
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755140
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