A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6248350



Internal ID22052960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94520789..94520789hg38UCSC Ensembl
chr11:94253955..94253955hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17843062
Samples
Known GenesLOC643037
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6248350
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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