A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842897



Internal ID22026540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74835408..74835408hg38UCSC Ensembl
chr10:76595166..76595166hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247257
Supporting Variants
Samples
Known GenesKAT6B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842897
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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