A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987447



Internal ID16281403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1010571..1031196hg38UCSC Ensembl
Innerchr4:1004359..1024984hg19UCSC Ensembl
Innerchr4:994359..1014984hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3820626
hg1920626
hg1820626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593235
Supporting Variants
Samples
Known GenesFGFRL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv987447
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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