A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395979



Internal ID22453849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19685876..19698085hg38UCSC Ensembl
chr19:19796685..19808894hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3812210
hg1912210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928652
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395979
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