A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977354



Internal ID52305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157954931..157955298hg38UCSC Ensembl
chr5:157381939..157382306hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455754
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977354
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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