A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6938140



Internal ID9988639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:72137141..72174624hg38UCSC Ensembl
Outerchr11:71848187..71885668hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3837484
hg1937482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744761
Supporting Variants
SamplesSSM003
Known GenesFOLR3
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)essv6938140
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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