A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2747353



Internal ID9981637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:45789339..45789567hg38UCSC Ensembl
Outerchr13:46363474..46363702hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6953392, essv6773642
SamplesSSM008, SSM025
Known GenesSIAH3
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)esv2747353
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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