A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6735058



Internal ID10145437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3654419..3654990hg38UCSC Ensembl
Outerchr11:3675649..3676220hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744040, esv2744043
Supporting Variants
SamplesSSM049
Known GenesART1
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)essv6735058
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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