A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374299



Internal ID22599968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68821767..68826161hg38UCSC Ensembl
chr17:66817908..66822302hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg384395
hg194395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374299
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