A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858269



Internal ID22041912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131612226..131612226hg38UCSC Ensembl
chr5:130947919..130947919hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244848
Supporting Variants
Samples
Known GenesRAPGEF6
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858269
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