A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6902176



Internal ID9664927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63757488..63758030hg38UCSC Ensembl
Outerchr20:62388841..62389383hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722959, esv2722967
Supporting Variants
SamplesSSM012
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)essv6902176
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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