A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3661434



Internal ID19379442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21723161..21723161hg38UCSC Ensembl
chr22:22077450..22077450hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16484494
Samples
Known GenesYPEL1
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)esv3661434
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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