A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6420n54



Internal ID18998596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35360012..35372126hg38UCSC Ensembl
chr19:35850914..35863028hg19UCSC Ensembl
chr19:40542754..40554868hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812115
hg1912115
hg1812115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579403, nsv579404
Samples
Known GenesFFAR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6420n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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