A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842984



Internal ID22026627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109365529..109365529hg38UCSC Ensembl
chr10:111125287..111125287hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842984
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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