A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047662



Internal ID20614702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32544477..32547210hg38UCSC Ensembl
chr19:33035383..33038116hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382734
hg192734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521252
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047662
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