A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv925n54



Internal ID20134349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1198080..1862404hg38UCSC Ensembl
chr10:1244020..1904598hg19UCSC Ensembl
chr10:1234020..1894598hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38664325
hg19660579
hg18660579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549769, nsv549786
Samples
Known GenesADARB2, ADARB2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv925n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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