A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589313



Internal ID16030036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1022142..1906428hg38UCSC Ensembl
Innerchr3:1063826..1948112hg19UCSC Ensembl
Innerchr3:1038826..1923112hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38884287
hg19884287
hg18884287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957821
Samples
Known GenesCNTN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589313
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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