A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv370e59



Internal ID20127119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12774847..12776345hg38UCSC Ensembl
chr10:12816846..12818344hg19UCSC Ensembl
chr10:12856852..12858350hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3450539, esv3410646, esv3432921, esv3431870
SamplesNA12891, NA12878, NA12892, NA19240
Known GenesCAMK1D
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv370e59
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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