A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5688998



Internal ID21715319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24211662..24211662hg38UCSC Ensembl
chr2:24434531..24434531hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17207063, nssv17198713
Samples
Known GenesITSN2
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)nsv5688998
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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