A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247756



Internal ID22052366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9460201..9460201hg38UCSC Ensembl
chr11:9481748..9481748hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842487
Samples
Known GenesLOC644656
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247756
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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