A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589386



Internal ID16030109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2478019..2542692hg38UCSC Ensembl
Innerchr3:2519703..2584376hg19UCSC Ensembl
Innerchr3:2494703..2559376hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3864674
hg1964674
hg1864674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8169n54
Supporting Variantsnssv957984
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589386
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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