A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593233



Internal ID16380642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1010433..1013136hg38UCSC Ensembl
Innerchr4:1004221..1006924hg19UCSC Ensembl
Innerchr4:994221..996924hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg382704
hg192704
hg182704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv987445
Samples
Known GenesFGFRL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593233
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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