A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561084



Internal ID16001807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132508641..132527419hg38UCSC Ensembl
Innerchr12:133085227..133104005hg19UCSC Ensembl
Innerchr12:131595300..131614078hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3818779
hg1918779
hg1818779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv805877
Samples
Known GenesFBRSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561084
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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