A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6945449



Internal ID9703142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:88855596..88855756hg38UCSC Ensembl
Outerchr15:89398827..89398987hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749997, esv2749995
Supporting Variants
SamplesSSM023
Known GenesACAN
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)essv6945449
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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