A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6932757



Internal ID10041770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:59590957..59591287hg38UCSC Ensembl
Outerchr18:57258189..57258519hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717169
Supporting Variants
SamplesSSM020
Known GenesCCBE1
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)essv6932757
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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