A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564907



Internal ID16005630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64544791..64551945hg38UCSC Ensembl
Innerchr14:65011509..65018663hg19UCSC Ensembl
Innerchr14:64081262..64088416hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg387155
hg197155
hg187155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828239
Samples
Known GenesPPP1R36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564907
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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