A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6806062



Internal ID9861466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:109667935..109668232hg38UCSC Ensembl
Outerchr9:112430215..112430512hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738914
Supporting Variants
SamplesSSM074
Known GenesPALM2
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)essv6806062
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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