A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592858



Internal ID16380267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192167253..192173334hg38UCSC Ensembl
Innerchr3:191885042..191891123hg19UCSC Ensembl
Innerchr3:193367736..193373817hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg386082
hg196082
hg186082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv984025
Samples
Known GenesFGF12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592858
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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