A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454344



Internal ID22512220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105725958..105728788hg38UCSC Ensembl
chr13:106378307..106381137hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg382831
hg192831
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860350
Supporting Variants
Samples
Known GenesLINC00343
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454344
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