A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17252976



Internal ID21700485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6641732..6641732hg38UCSC Ensembl
chr6:6641965..6641965hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5728635
Supporting Variants
Samples
Known GenesLY86
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)nssv17252976
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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