A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015759



Internal ID20582799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98064675..98066226hg38UCSC Ensembl
chr13:98716929..98718480hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488856
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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