A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3670271



Internal ID19388279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4157898..4157898hg38UCSC Ensembl
chr20:4138545..4138545hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16492448
Samples
Known GenesSMOX
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)esv3670271
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer