A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892531



Internal ID22667583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99149606..99151245hg38UCSC Ensembl
chr4:100070763..100072402hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381640
hg191640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416953
Samples
Known GenesLOC100507053
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892531
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