A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930642



Internal ID22705912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:23734396..25650314hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381915919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv902n209
Supporting Variantsnssv17386485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930642
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