A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589388



Internal ID16030111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2487316..2571317hg38UCSC Ensembl
Innerchr3:2529000..2613001hg19UCSC Ensembl
Innerchr3:2504000..2588001hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3884002
hg1984002
hg1884002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957986
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589388
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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