A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9014n54



Internal ID22776909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38663996..38665125hg38UCSC Ensembl
chr4:38665617..38666746hg19UCSC Ensembl
chr4:38342012..38343141hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381130
hg191130
hg181130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594004, nsv594002
Samples
Known GenesFLJ13197, KLF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9014n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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