A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469397



Internal ID22527287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99415536..99421010hg38UCSC Ensembl
chr13:100067790..100073264hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg385475
hg195475
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858838
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469397
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