A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255079



Internal ID22059689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103788455..103788455hg38UCSC Ensembl
chr4:104709612..104709612hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17855943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255079
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