A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841961



Internal ID22025604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97642825..97642825hg38UCSC Ensembl
chr10:99402582..99402582hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247412
Supporting Variants
Samples
Known GenesPI4K2A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841961
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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