A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6827505



Internal ID9881550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1873889..1874059hg38UCSC Ensembl
Outerchr11:1895119..1895289hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743970, esv2743971
Supporting Variants
SamplesSSM080
Known GenesLSP1
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)essv6827505
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