A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958884



Internal ID39894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158567692..158567742hg38UCSC Ensembl
chr4:159488844..159488894hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534593
Supporting Variants
Samples
Known GenesRXFP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958884
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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