A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6258250



Internal ID22062860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101866183..101866183hg38UCSC Ensembl
chr11:101736914..101736914hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17843453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6258250
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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