A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841817



Internal ID22025460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11927068..11927068hg38UCSC Ensembl
chr10:11969067..11969067hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240387
Supporting Variants
Samples
Known GenesUPF2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841817
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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