A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590918



Internal ID16031641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87274184..87861781hg38UCSC Ensembl
Innerchr3:87323334..87910931hg19UCSC Ensembl
Innerchr3:87406024..87993621hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38587598
hg19587598
hg18587598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967559
Samples
Known GenesPOU1F1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590918
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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