A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961529



Internal ID41656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3572315..3589606hg38UCSC Ensembl
chr5:3572429..3589720hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3817292
hg1917292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465022
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961529
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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