A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12n21



Internal ID22766204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102113751..102276919hg38UCSC Ensembl
chr1:102579307..102742475hg19UCSC Ensembl
chr1:102351895..102515063hg18UCSC Ensembl
chr1:102291328..102454496hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38163169
hg19163169
hg18163169
hg17163169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527496, nsv528450
Samples
Known GenesMIR548AI
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv12n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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