A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485628



Internal ID22543539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146202011..146204260hg38UCSC Ensembl
chr3:145919798..145922047hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382250
hg192250
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834969
Supporting Variants
Samples
Known GenesPLSCR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485628
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