A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5724390



Internal ID21750711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154539035..154539035hg38UCSC Ensembl
chrX:153767249..153767249hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17237871
Samples
Known GenesG6PD
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)nsv5724390
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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