A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3660545



Internal ID19378553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20083316..20083316hg38UCSC Ensembl
chr20:20063960..20063960hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16483694
Samples
Known GenesC20orf26
MethodSequencing
Analysisde novo assemblies produced from SoapDenovo2 were aligned to GRC37 using LAST and input into SoapAsmVar for population-wide structural variation detection. The method is described in the publication
PlatformIllumina HiSeq 2000
Comments
ReferenceBesenbacher_et_al_2015
Pubmed ID25597990
Accession Number(s)esv3660545
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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