A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3680322



Internal ID19398330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64271059..64271384hg38UCSC Ensembl
chr11:64038531..64038856hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16501494
Samples
Known GenesBAD
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)esv3680322
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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