A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945260



Internal ID30842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15909298..15956885hg38UCSC Ensembl
chr4:15910921..15958508hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3847588
hg1947588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451320
Supporting Variants
Samples
Known GenesFGFBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945260
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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