A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950105



Internal ID34090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54567687..54568868hg38UCSC Ensembl
chr4:55433854..55435035hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381182
hg191182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464493
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950105
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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