A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483280



Internal ID22541187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22578489..22597803hg38UCSC Ensembl
chr20:22559127..22578441hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3819315
hg1919315
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870306
Supporting Variants
Samples
Known GenesFOXA2, LINC00261
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483280
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