A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16491107



Internal ID19354667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31761337..31761337hg38UCSC Ensembl
chr11:31782885..31782885hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3668781
Supporting Variants
Samples
Known GenesELP4
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)essv16491107
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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