A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919482



Internal ID22694704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35145026..35146738hg38UCSC Ensembl
chr9:35145023..35146735hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381713
hg191713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919482
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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