A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6941337



Internal ID10049336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:60764178..60764476hg38UCSC Ensembl
Outerchr20:59339234..59339532hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722656
Supporting Variants
SamplesSSM022
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)essv6941337
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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