A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559211



Internal ID16346620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:66967877..67082126hg38UCSC Ensembl
Innerchr12:67361657..67475906hg19UCSC Ensembl
Innerchr12:65647924..65762173hg18UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38114250
hg19114250
hg18114250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv797560
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559211
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