A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17221809



Internal ID21669318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135416913..135416913hg38UCSC Ensembl
chr8:136429156..136429156hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5703929
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)nssv17221809
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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