A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016741



Internal ID20583781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23582182..23582374hg38UCSC Ensembl
chr14:24051391..24051583hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00699


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