A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952438



Internal ID35652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:78238351..78238351hg38UCSC Ensembl
chr4:79159505..79159505hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536525
Supporting Variants
Samples
Known GenesFRAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952438
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.589579


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