A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481966



Internal ID22539871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197893607..197896941hg38UCSC Ensembl
chr2:198758331..198761665hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg383335
hg193335
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831842
Supporting Variants
Samples
Known GenesPLCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481966
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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