A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv800472



Internal ID15747742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:91111068..91171917hg38UCSC Ensembl
Innerchr12:91504845..91565694hg19UCSC Ensembl
Innerchr12:90028976..90089825hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3860850
hg1960850
hg1860850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559751
Supporting Variants
Samples
Known GenesDCN, LUM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv800472
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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