A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6682482



Internal ID9748527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63757664..63757909hg38UCSC Ensembl
Outerchr20:62389017..62389262hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722959, esv2722967, esv2722968
Supporting Variants
SamplesSSM033
Known GenesZBTB46
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)essv6682482
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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