A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8902n54



Internal ID20142326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1797575..1807760hg38UCSC Ensembl
chr4:1799302..1809487hg19UCSC Ensembl
chr4:1769100..1779285hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3810186
hg1910186
hg1810186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593337, nsv593338
Samples
Known GenesFGFR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8902n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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