A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17188135



Internal ID21635644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44973898..44973898hg38UCSC Ensembl
chr10:45469346..45469346hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5705565
Supporting Variants
Samples
Known GenesRASSF4
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)nssv17188135
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