A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016497



Internal ID20583537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101192897..101194821hg38UCSC Ensembl
chr14:101659234..101661158hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381925
hg191925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016497
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