A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593234



Internal ID16380643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1010571..1022414hg38UCSC Ensembl
Innerchr4:1004359..1016202hg19UCSC Ensembl
Innerchr4:994359..1006202hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3811844
hg1911844
hg1811844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv987446
Samples
Known GenesFGFRL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593234
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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