A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960326



Internal ID40855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185823552..185823552hg38UCSC Ensembl
chr4:186744706..186744706hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548471
Supporting Variants
Samples
Known GenesSORBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960326
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.015729


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