A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976496



Internal ID51721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162396230..162400739hg38UCSC Ensembl
chr5:161823236..161827745hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg384510
hg194510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976496
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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