A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4589n100



Internal ID22790676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48767465..48787085hg38UCSC Ensembl
chr22:49163277..49182897hg19UCSC Ensembl
chr22:47549283..47568903hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3819621
hg1919621
hg1819621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066341, nsv1066760, nsv1063871, nsv1066347
Samples
Known GenesMIR4535
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4589n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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