A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989737



Internal ID60580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153538028..153538028hg38UCSC Ensembl
chr6:153859163..153859163hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394764
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.048887


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