A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259846



Internal ID22064456
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 StatusM
Merged Variants
Supporting Variantsnssv17854218
Samples
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259846
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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