A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842626



Internal ID22026269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102856240..102856240hg38UCSC Ensembl
chr10:104615997..104615997hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247449
Supporting Variants
Samples
Known GenesC10orf32, C10orf32-ASMT
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842626
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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