A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842234



Internal ID22025877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76941120..76941120hg38UCSC Ensembl
chr10:78700878..78700878hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247269
Supporting Variants
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842234
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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