A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6924786



Internal ID9687524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:89416297..89418411hg38UCSC Ensembl
Outerchr15:89959528..89961642hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382115
hg192115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750002
Supporting Variants
SamplesSSM018
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)essv6924786
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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