A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857771



Internal ID22041414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90702017..90702017hg38UCSC Ensembl
chr5:89997834..89997834hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244523
Supporting Variants
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857771
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