A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975402



Internal ID50990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166003012..166003142hg38UCSC Ensembl
chr5:165430017..165430147hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468000
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975402
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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