A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252179



Internal ID22056789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45341368..45341368hg38UCSC Ensembl
chr22:45737249..45737249hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850763
Samples
Known GenesFAM118A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252179
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