A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560160



Internal ID16000883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111034121..111035030hg38UCSC Ensembl
Innerchr12:111471925..111472834hg19UCSC Ensembl
Innerchr12:109956308..109957217hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38910
hg19910
hg18910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv802013, nssv802012, nssv802011
Samples
Known GenesCUX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560160
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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