A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5725986



Internal ID21752307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113876736..113876736hg38UCSC Ensembl
chr11:113747458..113747458hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17235423
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)nsv5725986
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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