A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6781455



Internal ID10186199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:45031667..45032062hg38UCSC Ensembl
Outerchr3:45073159..45073554hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2725216
Supporting Variants
SamplesSSM068
Known GenesCLEC3B
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)essv6781455
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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