A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6692306



Internal ID9758906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:78430808..78431407hg38UCSC Ensembl
Outerchr18:76190808..76191407hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717524, esv2717497, esv2717526
Supporting Variants
SamplesSSM036
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)essv6692306
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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