A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17187413



Internal ID21634922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75264346..75264346hg38UCSC Ensembl
chr9:77879262..77879262hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5698451
Supporting Variants
Samples
Known Genes
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)nssv17187413
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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