A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948105



Internal ID32767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40186282..40186282hg38UCSC Ensembl
chr4:40187902..40187902hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5403311
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948105
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.050048


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