A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589740



Internal ID16030463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13258336..13328202hg38UCSC Ensembl
Innerchr3:13299836..13369702hg19UCSC Ensembl
Innerchr3:13274836..13344702hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3869867
hg1969867
hg1869867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959225
Samples
Known GenesNUP210
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589740
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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