A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016409



Internal ID20583449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99314666..99319184hg38UCSC Ensembl
chr13:99966920..99971438hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384519
hg194519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476790
Supporting Variants
Samples
Known GenesMIR548AN, UBAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer