A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962844



Internal ID42551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16391683..16391734hg38UCSC Ensembl
chr5:16391792..16391843hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412076
Supporting Variants
Samples
Known GenesLOC101929505
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962844
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.082891


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