A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413768



Internal ID22471638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39157528..39174235hg38UCSC Ensembl
chr3:39199019..39215726hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3816708
hg1916708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895699
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413768
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