A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486733



Internal ID22544648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58386155..58387654hg38UCSC Ensembl
chr20:56961211..56962710hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486733
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