A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2737741



Internal ID10321377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:140098945..140099464hg38UCSC Ensembl
Outerchr8:141109044..141109563hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6782953, essv6712513, essv6894177
SamplesSSM042, SSM068, SSM012
Known GenesTRAPPC9
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)esv2737741
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