A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6819918



Internal ID10219532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:73500790..73501115hg38UCSC Ensembl
Outerchr13:74074927..74075252hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747640
Supporting Variants
SamplesSSM078
Known Genes
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)essv6819918
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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