A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564909



Internal ID16352318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64548937..64553549hg38UCSC Ensembl
Innerchr14:65015655..65020267hg19UCSC Ensembl
Innerchr14:64085408..64090020hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg384613
hg194613
hg184613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828241
Samples
Known GenesPPP1R36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564909
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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