A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17213792



Internal ID21661301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11384812..11384812hg38UCSC Ensembl
chrY:13540488..13540488hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5722552
Supporting Variants
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)nssv17213792
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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