A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560158



Internal ID16000881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111034121..111034664hg38UCSC Ensembl
Innerchr12:111471925..111472468hg19UCSC Ensembl
Innerchr12:109956308..109956851hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38544
hg19544
hg18544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2862n54
Supporting Variantsnssv802006, nssv802007
Samples
Known GenesCUX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560158
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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