A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423637



Internal ID22481507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2359408..2359559hg38UCSC Ensembl
chr5:2359522..2359673hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423637
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