A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462093



Internal ID22519978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100318898..100323014hg38UCSC Ensembl
chr13:100971152..100975268hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384117
hg194117
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851857
Supporting Variants
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462093
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