A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560567



Internal ID16001290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540458..124541327hg38UCSC Ensembl
Innerchr12:125025004..125025873hg19UCSC Ensembl
Innerchr12:123590957..123591826hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38870
hg19870
hg18870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2936n54
Supporting Variantsnssv804027
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560567
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