A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16491665



Internal ID19355225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55329134..55329134hg38UCSC Ensembl
chr14:55795852..55795852hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3669401
Supporting Variants
Samples
Known GenesFBXO34
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)essv16491665
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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