A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6849123



Internal ID9901006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32827748..32827854hg38UCSC Ensembl
Outerchr6:32795525..32795631hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731872, esv2731874
Supporting Variants
SamplesSSM086
Known GenesTAP2
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)essv6849123
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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