A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404516



Internal ID22462386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58188253..58189852hg38UCSC Ensembl
chr19:58699620..58701219hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938141
Supporting Variants
Samples
Known GenesZNF274
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404516
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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