A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6947933



Internal ID10056168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:163291041..163291323hg38UCSC Ensembl
Outerchr6:163712073..163712355hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733110
Supporting Variants
SamplesSSM024
Known GenesPACRG
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)essv6947933
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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