A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858871



Internal ID22042514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172098582..172098582hg38UCSC Ensembl
chr5:171525586..171525586hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256476
Supporting Variants
Samples
Known GenesSTK10
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858871
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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