A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426492



Internal ID22484362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170947169..170961113hg38UCSC Ensembl
chr3:170664958..170678902hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3813945
hg1913945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894299
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426492
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