A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6778878



Internal ID10184471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:115476014..115476331hg38UCSC Ensembl
Outerchr8:116488241..116488558hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2737465, esv2737464
Supporting Variants
SamplesSSM067
Known GenesTRPS1
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)essv6778878
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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