A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17197089



Internal ID21644598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60870925..60870925hg38UCSC Ensembl
chr15:61163124..61163124hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5696073
Supporting Variants
Samples
Known GenesRORA
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)nssv17197089
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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