A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975196



Internal ID50850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153919178..153948577hg38UCSC Ensembl
chr5:153298738..153328137hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3829400
hg1929400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465097
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975196
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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