A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940838



Internal ID22716252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10869944..10870956hg38UCSC Ensembl
chr19:10980620..10981632hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381013
hg191013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940838
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