A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3672086



Internal ID19390094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87239316..87239404hg38UCSC Ensembl
chr6:87949034..87949122hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16494081
Samples
Known GenesZNF292
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)esv3672086
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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