A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6835691



Internal ID9888731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:78517487..78517937hg38UCSC Ensembl
Outerchr18:76277487..76277937hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717497, esv2717550
Supporting Variants
SamplesSSM082
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)essv6835691
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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