A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009464



Internal ID22071095
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155027
Supporting Variants
Samples
Known GenesPPP1R36
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009464
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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