A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589381



Internal ID16030104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2453646..2454664hg38UCSC Ensembl
Innerchr3:2495330..2496348hg19UCSC Ensembl
Innerchr3:2470330..2471348hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381019
hg191019
hg181019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957917, nssv957919, nssv957918, nssv957915, nssv957914, nssv957916
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589381
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer