A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943080



Internal ID22718524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48675994..48677530hg38UCSC Ensembl
chr15:48968191..48969727hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943080
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