A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5700350



Internal ID21726671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131572027..131572027hg38UCSC Ensembl
chr11:131441921..131441921hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17191640
Samples
Known GenesNTM
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5700350
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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