A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960959



Internal ID41283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168474106..168474145hg38UCSC Ensembl
chr4:169395257..169395296hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547179
Supporting Variants
Samples
Known GenesDDX60L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960959
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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