A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946150



Internal ID22721636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45309513..45309819hg38UCSC Ensembl
chr19:45812771..45813077hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391906
Samples
Known GenesCKM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946150
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