A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560568



Internal ID16001291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540458..124541491hg38UCSC Ensembl
Innerchr12:125025004..125026037hg19UCSC Ensembl
Innerchr12:123590957..123591990hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381034
hg191034
hg181034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2941n54
Supporting Variantsnssv804029, nssv804028
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560568
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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