A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5720876



Internal ID21747197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105301286..105301286hg38UCSC Ensembl
chr7:104941733..104941733hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381971
hg191971
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17240389
Samples
Known GenesSRPK2
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)nsv5720876
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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