A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6258391



Internal ID22063001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118305556..118305556hg38UCSC Ensembl
chr11:118176271..118176271hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17843309
Samples
Known GenesCD3E
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6258391
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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