A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5691467



Internal ID21717788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93888608..93888608hg38UCSC Ensembl
chr7:93517920..93517920hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17182175
Samples
Known GenesTFPI2
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)nsv5691467
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