A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3678132



Internal ID19396140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86166188..86166242hg38UCSC Ensembl
chr7:85795504..85795558hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16499522
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)esv3678132
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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