A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617233



Internal ID21809280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90612907..90638644hg38UCSC Ensembl
chr12:91006684..91032421hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3825738
hg1925738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025167
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617233
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer