A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5698527



Internal ID21724848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12691038..12691038hg38UCSC Ensembl
chr12:12843972..12843972hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17219082, nssv17190804
Samples
Known GenesGPR19
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)nsv5698527
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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