A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6688195



Internal ID10102552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67710109..67990004hg38UCSC Ensembl
Outerchr11:67477580..67757475hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38279896
hg19279896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744651
Supporting Variants
SamplesSSM035
Known GenesFAM86C2P
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)essv6688195
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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