A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559850



Internal ID16347259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:97361343..97370466hg38UCSC Ensembl
Innerchr12:97755121..97764244hg19UCSC Ensembl
Innerchr12:96279252..96288375hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg389124
hg199124
hg189124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175740
SamplesHGDP00001
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559850
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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