A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962265



Internal ID42141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185056646..185056646hg38UCSC Ensembl
chr4:185977800..185977800hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5395035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962265
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.467928


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