A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17195864



Internal ID21643373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71997894..71997894hg38UCSC Ensembl
chr14:72464611..72464611hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5694520
Supporting Variants
Samples
Known GenesRGS6
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)nssv17195864
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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