A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3653823



Internal ID19371831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48799368..48799368hg38UCSC Ensembl
chr12:49193151..49193151hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16477644
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)esv3653823
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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