A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696955



Internal ID21723276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10924742..10924742hg38UCSC Ensembl
chr10:10966705..10966705hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17188385, nssv17218486
Samples
Known Genes
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)nsv5696955
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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