A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560575



Internal ID16001298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540561..124540719hg38UCSC Ensembl
Innerchr12:125025107..125025265hg19UCSC Ensembl
Innerchr12:123591060..123591218hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38159
hg19159
hg18159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv804110
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560575
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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