A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960956



Internal ID41282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168440433..168442186hg38UCSC Ensembl
chr4:169361584..169363337hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381754
hg191754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460874
Supporting Variants
Samples
Known GenesDDX60L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960956
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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