A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17194767



Internal ID21642276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38406226..38406226hg38UCSC Ensembl
chr14:38875430..38875430hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5697154
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)nssv17194767
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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