A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155011



Internal ID22085516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22453246..22514241hg38UCSC Ensembl
Outerchr14:22448641..22519044hg38UCSC Ensembl
Innerchr14:22922238..22983223hg19UCSC Ensembl
Outerchr14:22917633..22988022hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3870404
hg1970390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009413
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155011
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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