A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561102



Internal ID16001825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132511121..132553706hg38UCSC Ensembl
Innerchr12:133087707..133130292hg19UCSC Ensembl
Innerchr12:131597780..131640365hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3842586
hg1942586
hg1842586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3051n54
Supporting Variantsnssv805912
Samples
Known GenesFBRSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561102
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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