A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968111



Internal ID46052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85522497..85522590hg38UCSC Ensembl
chr5:84818315..84818408hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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