A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590399



Internal ID16377808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60402589..60659401hg38UCSC Ensembl
Innerchr3:60388322..60645134hg19UCSC Ensembl
Innerchr3:60363362..60620174hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38256813
hg19256813
hg18256813
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151898
Samples1782681329_A
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590399
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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