A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8901n54



Internal ID19001077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1644637..1864631hg38UCSC Ensembl
chr4:1646364..1866358hg19UCSC Ensembl
chr4:1616181..1836156hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38219995
hg19219995
hg18219976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593336, nsv593335
Samples
Known GenesFAM53A, FGFR3, LETM1, SLBP, TACC3, TMEM129
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8901n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer