A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17215367



Internal ID21662876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95851739..95851739hg38UCSC Ensembl
chr9:98614021..98614021hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5709194
Supporting Variants
Samples
Known GenesLINC00476
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)nssv17215367
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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