A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17209049



Internal ID21656558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119935460..119935460hg38UCSC Ensembl
chr2:120693036..120693036hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5679313
Supporting Variants
Samples
Known GenesPTPN4
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)nssv17209049
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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