A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17226013



Internal ID21673522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108595476..108595476hg38UCSC Ensembl
chr9:111357756..111357756hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg388228
hg198228
Variant TypeCNV herv insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5699850
Supporting Variants
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a HERV mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17226013
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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