A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049899



Internal ID20616939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58359203..58361895hg38UCSC Ensembl
chr19:58870569..58873261hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382693
hg192693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525521
Supporting Variants
Samples
Known GenesZNF497
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049899
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