A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971333



Internal ID48233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90441984..90444560hg38UCSC Ensembl
chr5:89737801..89740377hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg382577
hg192577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458391
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971333
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008901


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