A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2738897



Internal ID9973238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:107289061..107289249hg38UCSC Ensembl
Outerchr9:110051342..110051530hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6856512
SamplesSSM087
Known GenesRAD23B
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)esv2738897
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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