A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6666164



Internal ID9733011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79740026..79740119hg38UCSC Ensembl
Outerchr18:77500026..77500119hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717683, esv2717682
Supporting Variants
SamplesSSM029
Known GenesCTDP1
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)essv6666164
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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