A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735328



Internal ID158994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15738058..15742610hg38UCSC Ensembl
chr5:15738167..15742719hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg384553
hg194553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457505
Supporting Variants
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735328
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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