A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956529



Internal ID38325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145299733..145300352hg38UCSC Ensembl
chr4:146220885..146221504hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458551
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956529
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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