A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154976



Internal ID22085481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18552524..18693043hg38UCSC Ensembl
Outerchr14:18497148..18955961hg38UCSC Ensembl
Innerchr14:19329001..19469520hg19UCSC Ensembl
Outerchr14:19273625..19541714hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38458814
hg19268090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008314
Samples
Known GenesLOC642426, OR11H12
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154976
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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