A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593769



Internal ID16381178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15919848..15941517hg38UCSC Ensembl
Innerchr4:15921471..15943140hg19UCSC Ensembl
Innerchr4:15530569..15552238hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3821670
hg1921670
hg1821670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv993097
Samples
Known GenesFGFBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593769
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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