A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17190834



Internal ID21638343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14802350..14802350hg38UCSC Ensembl
chr12:14955284..14955284hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5706176
Supporting Variants
Samples
Known GenesWBP11
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)nssv17190834
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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