A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1n21



Internal ID20131722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3391470..3398032hg38UCSC Ensembl
chr1:3308034..3314596hg19UCSC Ensembl
chr1:3297894..3304456hg18UCSC Ensembl
chr1:3331191..3337753hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg386563
hg196563
hg186563
hg176563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527139, nsv521921
Samples
Known GenesPRDM16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv1n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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