A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975258



Internal ID50892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154657260..154657296hg38UCSC Ensembl
chr5:154036820..154036856hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544996
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975258
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.066677


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