A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17241329



Internal ID21688838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55198152..55198152hg38UCSC Ensembl
chr1:55663825..55663825hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5726851
Supporting Variants
Samples
Known GenesUSP24
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a L1 mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17241329
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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