A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5699375



Internal ID21725696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50955801..50955801hg38UCSC Ensembl
chr13:51529937..51529937hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17194495
Samples
Known GenesRNASEH2B
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)nsv5699375
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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