A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958729



Internal ID39797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156804268..156804319hg38UCSC Ensembl
chr4:157725420..157725471hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5396898
Supporting Variants
Samples
Known GenesPDGFC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958729
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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