A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5721590



Internal ID21747911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76877668..76877668hg38UCSC Ensembl
chr6:77587385..77587385hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg386008
hg196008
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17237946
Samples
Known Genes
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)nsv5721590
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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