A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5707439



Internal ID21733760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95704168..95704168hg38UCSC Ensembl
chr8:96716396..96716396hg19UCSC Ensembl
Cytoband8q22.1
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 Variantsnssv17230639, nssv17184831
Samples
Known GenesLOC100616530
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)nsv5707439
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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