A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17244297



Internal ID21691806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214647394..214647394hg38UCSC Ensembl
chr1:214820737..214820737hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5724464
Supporting Variants
Samples
Known GenesCENPF
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)nssv17244297
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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