A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590388



Internal ID16377797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59971526..60032600hg38UCSC Ensembl
Innerchr3:59957252..60018326hg19UCSC Ensembl
Innerchr3:59932292..59993366hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3861075
hg1961075
hg1861075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963386
Samples
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590388
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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