A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487070



Internal ID22544985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16611315..16617264hg38UCSC Ensembl
chr3:16652822..16658771hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385950
hg195950
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835094
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487070
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer