A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6248034



Internal ID22052644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43333940..43333940hg38UCSC Ensembl
chr11:43355490..43355490hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842393
Samples
Known GenesAPI5
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6248034
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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