A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6813665



Internal ID9658252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63770605..63771265hg38UCSC Ensembl
Outerchr20:62401958..62402618hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722970, esv2722959
Supporting Variants
SamplesSSM009
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)essv6813665
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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