A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16477077



Internal ID19340637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107401229..107401229hg38UCSC Ensembl
chr11:107271955..107271955hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3653192
Supporting Variants
Samples
Known GenesCWF19L2
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)essv16477077
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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