A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735373



Internal ID159039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57325185..57325300hg38UCSC Ensembl
chr5:56621012..56621127hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735373
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004527


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