A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405514



Internal ID22463384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31898688..31898797hg38UCSC Ensembl
chr19:32389594..32389703hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931492
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405514
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