A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049859



Internal ID20616899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58142665..58147915hg38UCSC Ensembl
chr19:58654032..58659282hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385251
hg195251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524695
Supporting Variants
Samples
Known GenesZNF329
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049859
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