A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5720352



Internal ID21746673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120133419..120133419hg38UCSC Ensembl
chrX:119267329..119267329hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17235908, nssv17236025
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)nsv5720352
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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