A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6245741



Internal ID22050351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22638451..22638451hg38UCSC Ensembl
chr8:22495964..22495964hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17839896
Samples
Known GenesBIN3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6245741
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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