A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406578



Internal ID22464448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33393160..33393265hg38UCSC Ensembl
chr19:33884066..33884171hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931770
Supporting Variants
Samples
Known GenesPEPD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406578
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer