A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5727769



Internal ID21754090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122075354..122075354hg38UCSC Ensembl
chrX:121209207..121209207hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17215134, nssv17205461
Samples
Known Genes
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)nsv5727769
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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