A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5730897



Internal ID21757218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105801734..105801734hg38UCSC Ensembl
chr11:105672460..105672460hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17240944
Samples
Known GenesGRIA4
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)nsv5730897
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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