A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927368



Internal ID18955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:178232016..178232067hg38UCSC Ensembl
chr2:179096743..179096794hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5397213
Supporting Variants
Samples
Known GenesOSBPL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927368
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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