A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5676128



Internal ID21702449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158893641..158893641hg38UCSC Ensembl
chr4:159814793..159814793hg19UCSC Ensembl
Cytoband4q32.1
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 Variantsnssv17212589, nssv17175737
Samples
Known GenesC4orf45, FNIP2
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)nsv5676128
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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