A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945241



Internal ID30828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15662167..15662269hg38UCSC Ensembl
chr4:15663790..15663892hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448486
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945241
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002968


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