A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057119



Internal ID19146338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11932018..12014705hg38UCSC Ensembl
Innerchr20:11912666..11995353hg19UCSC Ensembl
Innerchr20:11860666..11943353hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3882688
hg1982688
hg1882688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599380, nssv3599381
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)nsv1057119
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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