A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560298



Internal ID16347707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115176003..115203918hg38UCSC Ensembl
Innerchr12:115613808..115641723hg19UCSC Ensembl
Innerchr12:114098191..114126106hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3827916
hg1927916
hg1827916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv802795
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560298
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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