A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2717617



Internal ID9951908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:78964801..78965717hg38UCSC Ensembl
Outerchr18:76724801..76725717hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6913490, essv6832127, essv6921127, essv6801151, essv6721528, essv6703369, essv6960732, essv6784469, essv6717678, essv6824480, essv6780327, essv6932798, essv6916928, essv6895412
SamplesSSM079, SSM039, SSM026, SSM017, SSM067, SSM044, SSM068, SSM081, SSM072, SSM020, SSM015, SSM016, SSM043, SSM098
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)esv2717617
Frequency
Sample Size96
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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