A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6771999



Internal ID9832557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132069233..132069519hg38UCSC Ensembl
Outerchr11:131939127..131939413hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745277
Supporting Variants
SamplesSSM065
Known GenesNTM
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)essv6771999
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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