A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947102



Internal ID32097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28909781..28909832hg38UCSC Ensembl
chr4:28911403..28911454hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398233
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947102
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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