A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6246010



Internal ID22050620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54966100..54966100hg38UCSC Ensembl
chr8:55878660..55878660hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17839626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6246010
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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