A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3656349



Internal ID19374357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44767053..44767053hg38UCSC Ensembl
chr15:45059251..45059251hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16479918
Samples
Known GenesTRIM69
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)esv3656349
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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