A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951059



Internal ID34731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53578935..53578986hg38UCSC Ensembl
chr4:54445102..54445153hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5400658
Supporting Variants
Samples
Known GenesLNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951059
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010147


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