A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6870628



Internal ID9920363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:49403541..49403871hg38UCSC Ensembl
Outerchr11:49425093..49425423hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744485, esv2744501
Supporting Variants
SamplesSSM090
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)essv6870628
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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