A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962199



Internal ID42097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184376069..184376111hg38UCSC Ensembl
chr4:185297223..185297265hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5413276
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962199
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003746


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