A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589396



Internal ID16030119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3203825..3821595hg38UCSC Ensembl
Innerchr3:3245509..3863279hg19UCSC Ensembl
Innerchr3:3220509..3838279hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38617771
hg19617771
hg18617771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957994
Samples
Known GenesLRRN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589396
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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