A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv86e201



Internal ID20124973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3115013..3115353hg38UCSC Ensembl
chr10:3157205..3157545hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2731239, esv2731195
SamplesSSM045, SSM089, SSM001, SSM016
Known GenesPFKP
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)dgv86e201
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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