A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854218



Internal ID22037861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156228323..156228323hg38UCSC Ensembl
chr3:155946112..155946112hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259846
Supporting Variants
Samples
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854218
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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