A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5723993



Internal ID21750314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65219908..65219908hg38UCSC Ensembl
chr15:65512246..65512246hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17236195
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a SVA mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5723993
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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