A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv805914



Internal ID16099870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132579293..132602515hg38UCSC Ensembl
Innerchr12:133155879..133179101hg19UCSC Ensembl
Innerchr12:131665952..131689174hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3823223
hg1923223
hg1823223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561107
Supporting Variants
Samples
Known GenesFBRSL1, MIR6763
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv805914
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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