A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6732942



Internal ID10142841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:26450537..26452557hg38UCSC Ensembl
Outerchr18:24030501..24032521hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382021
hg192021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716883
Supporting Variants
SamplesSSM047
Known Genes
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)essv6732942
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