A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6839456



Internal ID9892495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:77969183..77969353hg38UCSC Ensembl
Outerchr18:75681139..75681309hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717388, esv2717481
Supporting Variants
SamplesSSM083
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)essv6839456
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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