A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958865



Internal ID39885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158363000..158611381hg38UCSC Ensembl
chr4:159284152..159532533hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38248382
hg19248382
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468710
Supporting Variants
Samples
Known GenesRXFP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958865
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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