A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17199263



Internal ID21646772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27919751..27919751hg38UCSC Ensembl
chr2:28142618..28142618hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5685276
Supporting Variants
Samples
Known GenesBRE
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)nssv17199263
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