A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5701990



Internal ID21728311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34986102..34986102hg38UCSC Ensembl
chr9:34986099..34986099hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17186134
Samples
Known GenesLOC101926900
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)nsv5701990
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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