A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5694499



Internal ID21720820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19964599..19964599hg38UCSC Ensembl
chr17:19867912..19867912hg19UCSC Ensembl
Cytoband17p11.2
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 Variantsnssv17197367
Samples
Known GenesAKAP10
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)nsv5694499
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