A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549146



Internal ID15989869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212285280..212286221hg38UCSC Ensembl
Innerchr1:212458622..212459563hg19UCSC Ensembl
Innerchr1:210525245..210526186hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38942
hg19942
hg18942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv804n54
Supporting Variantsnssv736859
Samples
Known GenesPPP2R5A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549146
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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