A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687785



Internal ID111451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52262106..52280106hg38UCSC Ensembl
chr13:52836241..52854241hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3818001
hg1918001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419056
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687785
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.463958


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