A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv802020



Internal ID15749290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111034274..111035030hg38UCSC Ensembl
Innerchr12:111472078..111472834hg19UCSC Ensembl
Innerchr12:109956461..109957217hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38757
hg19757
hg18757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560165
Supporting Variants
Samples
Known GenesCUX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv802020
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