A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6792826



Internal ID10195067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:40460207..40460424hg38UCSC Ensembl
Outerchr20:39088847..39089064hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722413
Supporting Variants
SamplesSSM070
Known Genes
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)essv6792826
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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