A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859463



Internal ID22043106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98383121..98383121hg38UCSC Ensembl
chr6:98830997..98830997hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859463
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