A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560574



Internal ID16001297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540458..124548792hg38UCSC Ensembl
Innerchr12:125025004..125033338hg19UCSC Ensembl
Innerchr12:123590957..123599291hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg388335
hg198335
hg188335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv804109
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560574
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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