A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449915



Internal ID22507786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68914513..68918353hg38UCSC Ensembl
chr13:69488645..69492485hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg383841
hg193841
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449915
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