A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5703570



Internal ID21729891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21741533..21741533hg38UCSC Ensembl
chr10:22030462..22030462hg19UCSC Ensembl
Cytoband10p12.31
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 Variantsnssv17188030
Samples
Known GenesMLLT10
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)nsv5703570
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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