A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17236362



Internal ID21683871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101845758..101845758hg38UCSC Ensembl
chr10:103605515..103605515hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5717552
Supporting Variants
Samples
Known GenesC10orf76
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)nssv17236362
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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