A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3656479



Internal ID19374487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59346867..59346867hg38UCSC Ensembl
chr15:59639066..59639066hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16480035
Samples
Known GenesMYO1E
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)esv3656479
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