A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv805869



Internal ID16099825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132508641..132510697hg38UCSC Ensembl
Innerchr12:133085227..133087283hg19UCSC Ensembl
Innerchr12:131595300..131597356hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg382057
hg192057
hg182057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561079
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)nssv805869
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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