A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954104



Internal ID36731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118838938..118843471hg38UCSC Ensembl
chr4:119760093..119764626hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg384534
hg194534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954104
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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