A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17186214



Internal ID21633723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123707884..123707884hg38UCSC Ensembl
chr8:124720124..124720124hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5705274
Supporting Variants
Samples
Known GenesANXA13
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)nssv17186214
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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