A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063259



Internal ID19152478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19269053..19315908hg38UCSC Ensembl
Innerchr21:20641370..20688225hg19UCSC Ensembl
Innerchr21:19563241..19610096hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3846856
hg1946856
hg1846856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599819
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)nsv1063259
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