A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17237838



Internal ID21685347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10942787..10942787hg38UCSC Ensembl
chr6:10943020..10943020hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg385327
hg195327
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5725700
Supporting Variants
Samples
Known GenesSYCP2L
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)nssv17237838
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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