A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945288



Internal ID30866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1026082..1026310hg38UCSC Ensembl
chr4:1019870..1020098hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452773
Supporting Variants
Samples
Known GenesFGFRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945288
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.124102


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