A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9389n54



Internal ID22777284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171455069..171575775hg38UCSC Ensembl
chr4:172376220..172496926hg19UCSC Ensembl
chr4:172612795..172733501hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38120707
hg19120707
hg18120707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596192, nsv596195, nsv596185, nsv596194, nsv596193
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9389n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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