A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057889



Internal ID19147108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:50907598..50950216hg38UCSC Ensembl
Innerchr17:48984959..49027577hg19UCSC Ensembl
Innerchr17:46339958..46382576hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3842619
hg1942619
hg1842619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568607
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)nsv1057889
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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