A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2724463



Internal ID10308099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:47028192..47028743hg38UCSC Ensembl
Outerchr22:47424088..47424639hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6668816, essv6937487, essv6747309, essv6666690, essv6674990, essv6858960, essv6909900, essv6773280, essv6699481, essv6967672
SamplesSSM027, SSM065, SSM087, SSM038, SSM021, SSM029, SSM031, SSM014, SSM007, SSM030
Known GenesTBC1D22A
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)esv2724463
Frequency
Sample Size96
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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