A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3649249



Internal ID19367257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65363265..65363320hg38UCSC Ensembl
chr14:65829983..65830038hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16473527
Samples
Known Genes
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)esv3649249
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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