A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2716970



Internal ID9951259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:37441807..37442202hg38UCSC Ensembl
Outerchr18:35021770..35022165hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6666028, essv6960620, essv6696415, essv6828485
SamplesSSM029, SSM026, SSM080, SSM037
Known GenesCELF4
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)esv2716970
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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