A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460084



Internal ID22517970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50870553..50872193hg38UCSC Ensembl
chr13:51444689..51446329hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381641
hg191641
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460084
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