A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709433



Internal ID133099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56721026..56721077hg38UCSC Ensembl
chr16:56754938..56754989hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424472
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709433
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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