A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5679849



Internal ID21706170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132204796..132204796hg38UCSC Ensembl
chr5:131540489..131540489hg19UCSC Ensembl
Cytoband5q31.1
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 Variantsnssv17178987
Samples
Known GenesP4HA2
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)nsv5679849
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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