A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3658013



Internal ID19376021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3673392..3673517hg38UCSC Ensembl
chr6:3673626..3673751hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16481415
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)esv3658013
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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