A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6826479



Internal ID9880627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:110749860..110750345hg38UCSC Ensembl
Outerchr6:111071063..111071548hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732571
Supporting Variants
SamplesSSM080
Known GenesCDK19
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)essv6826479
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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