A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5730876



Internal ID21757197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65670941..65670941hg38UCSC Ensembl
chrX:64890802..64890802hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17203350
Samples
Known GenesMSN
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5730876
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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