A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247362



Internal ID22051972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89701952..89701952hg38UCSC Ensembl
chr10:91461709..91461709hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841766
Samples
Known GenesKIF20B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247362
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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