A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv21n97



Internal ID22815418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172946563..173172552hg38UCSC Ensembl
chr1:172915703..173141691hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38225990
hg19225989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154345, nsv1154340
Samples
Known GenesTNFSF18
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv21n97
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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