A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590387



Internal ID16377796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59905250..60495726hg38UCSC Ensembl
Innerchr3:59890976..60481459hg19UCSC Ensembl
Innerchr3:59866016..60456499hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38590477
hg19590484
hg18590484
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963385
Samples
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590387
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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