A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481934



Internal ID22539839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:194633815..194666611hg38UCSC Ensembl
chr2:195498539..195531335hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3832797
hg1932797
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481934
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