A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564908



Internal ID16352317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64548937..64550756hg38UCSC Ensembl
Innerchr14:65015655..65017474hg19UCSC Ensembl
Innerchr14:64085408..64087227hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381820
hg191820
hg181820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828240
Samples
Known GenesPPP1R36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564908
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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