A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451006



Internal ID22508879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90840106..90843364hg38UCSC Ensembl
chr13:91492360..91495618hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg383259
hg193259
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858518
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451006
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