A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6258331



Internal ID22062941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110154852..110154852hg38UCSC Ensembl
chr11:110025577..110025577hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17843526
Samples
Known GenesZC3H12C
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6258331
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer