A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17217836



Internal ID21665345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119693044..119693044hg38UCSC Ensembl
chr12:120130849..120130849hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5696123
Supporting Variants
Samples
Known GenesCIT
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)nssv17217836
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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