A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10240n54



Internal ID20143664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179793009..179804681hg38UCSC Ensembl
chr5:179220010..179231681hg19UCSC Ensembl
chr5:179152616..179164287hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3811673
hg1911672
hg1811672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600666, nsv600662, nsv600665
Samples
Known GenesLTC4S, MGAT4B, MIR1229
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10240n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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