A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3672891



Internal ID19044213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93747032..93747033hg38UCSC Ensembl
chr11:93480198..93480199hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382
hg192
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16494805
Samples
Known GenesC11orf54
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)esv3672891
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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