A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590212



Internal ID16030935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:47443539..47459172hg38UCSC Ensembl
Innerchr3:47485029..47500662hg19UCSC Ensembl
Innerchr3:47460033..47475666hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3815634
hg1915634
hg1815634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962611
Samples
Known GenesSCAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590212
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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