A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974737



Internal ID50537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149457903..149493299hg38UCSC Ensembl
chr5:148837466..148872862hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3835397
hg1935397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457699
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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