A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv181n54



Internal ID22768076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22562710..22564576hg38UCSC Ensembl
chr1:22889203..22891069hg19UCSC Ensembl
chr1:22761790..22763656hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381867
hg191867
hg181867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545751, nsv545752
Samples
Known GenesEPHA8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv181n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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