A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17204699



Internal ID21652208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150818877..150818877hg38UCSC Ensembl
chr1:150791353..150791353hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5689479
Supporting Variants
Samples
Known GenesARNT
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)nssv17204699
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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