A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5728635



Internal ID21754956
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 StatusM
Merged Variants
Supporting Variantsnssv17252976
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)nsv5728635
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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