A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5555n100



Internal ID22791642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5679964..5719362hg38UCSC Ensembl
chr5:5680077..5719475hg19UCSC Ensembl
chr5:5733077..5772475hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3839399
hg1939399
hg1839399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023730, nsv1021821, nsv1025199, nsv1015279, nsv1028327, nsv1032925, nsv1016509, nsv1030475, nsv1025827, nsv1018150, nsv1018195, nsv1020489, nsv1020311, nsv1027651, nsv1024143, nsv1016160, nsv1027559
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5555n100
Frequency
Sample Size11257
Observed Gain76
Observed Loss0
Observed Complex0
Frequencyn/a


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