A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241658



Internal ID22046268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88593875..88593875hg38UCSC Ensembl
chr14:89060219..89060219hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846398
Samples
Known GenesZC3H14
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241658
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