A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945506



Internal ID31002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10631070..10631121hg38UCSC Ensembl
chr4:10632694..10632745hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562884
Supporting Variants
Samples
Known GenesCLNK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945506
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.020145


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