A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974369



Internal ID50282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133575187..133577371hg38UCSC Ensembl
chr5:132910878..132913062hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382185
hg192185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466490
Supporting Variants
Samples
Known GenesFSTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974369
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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