A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961496



Internal ID41636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3312347..3312796hg38UCSC Ensembl
chr5:3312461..3312910hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463544
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961496
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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