A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18012162



Internal ID20579202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68848401..68849800hg38UCSC Ensembl
chr13:69422533..69423932hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476838
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18012162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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