A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6937086



Internal ID9695853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:76423311..76424036hg38UCSC Ensembl
Outerchr18:74135267..74135992hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717388, esv2717394
Supporting Variants
SamplesSSM021
Known GenesZNF516
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)essv6937086
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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