A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1050n106



Internal ID22794878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19684741..19956441hg38UCSC Ensembl
chr14:20152900..20424600hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38271701
hg19271701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1124684, nsv1118534
SamplesKWS2, KWS1
Known GenesOR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1050n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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