A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2744649



Internal ID9978933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67670011..67670199hg38UCSC Ensembl
Outerchr11:67437482..67437670hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6758150, essv6959090
SamplesSSM026, SSM059
Known GenesALDH3B2
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)esv2744649
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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