A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480688



Internal ID22538592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174531704..174534031hg38UCSC Ensembl
chr2:175396432..175398759hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg382328
hg192328
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480688
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