A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5701125



Internal ID21727446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120625174..120625174hg38UCSC Ensembl
chr8:121637414..121637414hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17186168
Samples
Known GenesSNTB1
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)nsv5701125
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