A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3668149



Internal ID19386157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48540793..48540858hg38UCSC Ensembl
chr3:48578226..48578291hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16490538
Samples
Known GenesPFKFB4
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)esv3668149
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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