A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6916767



Internal ID9680982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:30905857..30906339hg38UCSC Ensembl
Outerchr17:29232875..29233357hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2715813, esv2715816
Supporting Variants
SamplesSSM016
Known GenesTEFM
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)essv6916767
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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