A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3683360



Internal ID19054682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57429504..57429800hg38UCSC Ensembl
chr16:57463416..57463712hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16463781
Samples
Known GenesCIAPIN1
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)esv3683360
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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