A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255458



Internal ID22060068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145037430..145037430hg38UCSC Ensembl
chr4:145958582..145958582hg19UCSC Ensembl
Cytoband4q31.21
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 Variantsnssv17856072
Samples
Known GenesANAPC10
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255458
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