A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5660n100



Internal ID22791747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:50159790..50185338hg38UCSC Ensembl
chr5:49455624..49481172hg19UCSC Ensembl
chr5:49491381..49516929hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3825549
hg1925549
hg1825549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017236, nsv1021169
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)dgv5660n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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