A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592511



Internal ID16379920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172163909..172175076hg38UCSC Ensembl
Innerchr3:171881699..171892866hg19UCSC Ensembl
Innerchr3:173364393..173375560hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3811168
hg1911168
hg1811168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8729n54
Supporting Variantsnssv981217
Samples
Known GenesFNDC3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592511
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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