A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6908809



Internal ID10018609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:134045961..134046305hg38UCSC Ensembl
Outerchr11:133915856..133916200hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745311
Supporting Variants
SamplesSSM014
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)essv6908809
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