A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155027



Internal ID22085532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64548935..64552811hg38UCSC Ensembl
Outerchr14:64546073..64559524hg38UCSC Ensembl
Innerchr14:65015653..65019529hg19UCSC Ensembl
Outerchr14:65012791..65026242hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3813452
hg1913452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009464
Samples
Known GenesPPP1R36
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155027
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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