A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022694



Internal ID20589734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90352665..90362103hg38UCSC Ensembl
chr14:90819009..90828447hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg389439
hg199439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022694
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