A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3671733



Internal ID19389741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6652055..6652069hg38UCSC Ensembl
chr6:6652288..6652302hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3815
hg1915
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16493763
Samples
Known GenesLY86
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)esv3671733
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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