A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5726644



Internal ID21752965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103594740..103594740hg38UCSC Ensembl
chr14:104061077..104061077hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381187
hg191187
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17252661
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)nsv5726644
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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