A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842260



Internal ID22025903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:208221407..208221407hg38UCSC Ensembl
chr1:208394752..208394752hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258090
Supporting Variants
Samples
Known GenesPLXNA2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842260
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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