A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16943988



Internal ID29985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2772422..2779293hg38UCSC Ensembl
chr4:2774149..2781020hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg386872
hg196872
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16943988
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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