A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241676



Internal ID22046286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90490545..90490545hg38UCSC Ensembl
chr14:90956889..90956889hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241676
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