A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv805909



Internal ID15753179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132510110..132512278hg38UCSC Ensembl
Innerchr12:133086696..133088864hg19UCSC Ensembl
Innerchr12:131596769..131598937hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg382169
hg192169
hg182169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561099
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)nssv805909
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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