A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493860



Internal ID22551790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121819052..121843425hg38UCSC Ensembl
chr5:121154747..121179120hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3824374
hg1924374
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841266
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493860
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer