A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6248827



Internal ID22053437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26664157..26664157hg38UCSC Ensembl
chr13:27238294..27238294hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17844743
Samples
Known GenesWASF3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6248827
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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