A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv805911



Internal ID15753181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132510697..132543723hg38UCSC Ensembl
Innerchr12:133087283..133120309hg19UCSC Ensembl
Innerchr12:131597356..131630382hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3833027
hg1933027
hg1833027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561101
Supporting Variants
Samples
Known GenesFBRSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv805911
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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