A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17177179



Internal ID21624688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178873581..178873581hg38UCSC Ensembl
chr5:178300582..178300582hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5675241
Supporting Variants
Samples
Known GenesZNF354B
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17177179
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer