A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3661037



Internal ID19379045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17103837..17104287hg38UCSC Ensembl
chr22:17584727..17585177hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16484137
Samples
Known GenesIL17RA
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)esv3661037
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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