A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475265



Internal ID22533160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36023515..36026364hg38UCSC Ensembl
chr19:36514417..36517266hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382850
hg192850
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869355
Supporting Variants
Samples
Known GenesCLIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475265
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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