A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1059n106



Internal ID20160416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28766394..28767994hg38UCSC Ensembl
chr14:29235600..29237200hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1118279, nsv1121872
SamplesKWS2, KWS1
Known GenesFOXG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1059n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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