A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5710761



Internal ID21737082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72073413..72073413hg38UCSC Ensembl
chr17:70069554..70069554hg19UCSC Ensembl
Cytoband17q24.3
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 Variantsnssv17200700, nssv17228186
Samples
Known GenesSOX9-AS1
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)nsv5710761
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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