A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5725673



Internal ID21751994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169089055..169089055hg38UCSC Ensembl
chr5:168516060..168516060hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17237101
Samples
Known GenesSLIT3
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a SVA mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5725673
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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