A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2737786



Internal ID9972125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:141445467..141445756hg38UCSC Ensembl
Outerchr8:142455567..142455856hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6705716, essv6948506, essv6841916
SamplesSSM024, SSM084, SSM040
Known GenesMROH5
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)esv2737786
Frequency
Sample Size96
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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