A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6827639



Internal ID10228357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:115678265..115678359hg38UCSC Ensembl
Outerchr11:115548983..115549077hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745105, esv2745104
Supporting Variants
SamplesSSM080
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)essv6827639
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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