A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2738859



Internal ID9973200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:103014585..103014790hg38UCSC Ensembl
Outerchr9:105776867..105777072hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6811906, essv6783069, essv6856503, essv6923860
SamplesSSM087, SSM068, SSM018, SSM076
Known GenesCYLC2
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)esv2738859
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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