A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409590



Internal ID22467460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134224640..134224692hg38UCSC Ensembl
chr3:133943484..133943536hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897506
Supporting Variants
Samples
Known GenesRYK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409590
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