A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17178684



Internal ID21626193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115321874..115321874hg38UCSC Ensembl
chr1:115864495..115864495hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5690922
Supporting Variants
Samples
Known GenesNGF
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)nssv17178684
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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