A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6245755



Internal ID22050365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24270784..24270784hg38UCSC Ensembl
chr8:24128297..24128297hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17840534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6245755
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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