A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3500n100



Internal ID20155116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27257073..27923726hg38UCSC Ensembl
chr19:27747981..28414634hg19UCSC Ensembl
chr19:32439821..33106474hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38666654
hg19666654
hg18666654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060674, nsv1060017, nsv1059366, nsv1060889, nsv1066699
Samples
Known GenesLINC00662
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3500n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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