A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5709598



Internal ID21735919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35693814..35693814hg38UCSC Ensembl
chr18:33273778..33273778hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17201495
Samples
Known GenesGALNT1
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)nsv5709598
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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