A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5913n100



Internal ID22792000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5144960..5200567hg38UCSC Ensembl
chr6:5145194..5200801hg19UCSC Ensembl
chr6:5090193..5145800hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3855608
hg1955608
hg1855608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022336, nsv1018984
Samples
Known GenesLYRM4, MIR3691
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5913n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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