A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv929n54



Internal ID20134353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1237571..1240333hg38UCSC Ensembl
chr10:1281487..1282372hg19UCSC Ensembl
chr10:1271487..1272372hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg382763
hg19886
hg18886
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549780, nsv549775
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv929n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss9
Observed Complex0
Frequencyn/a


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