A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6674552



Internal ID9742377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79742074..79742189hg38UCSC Ensembl
Outerchr18:77502074..77502189hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717687, esv2717688
Supporting Variants
SamplesSSM031
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)essv6674552
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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