A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368532



Internal ID22594201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110414557..110416414hg38UCSC Ensembl
chr12:110852362..110854219hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg381858
hg191858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368532
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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