A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059465



Internal ID19148684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13744391..13975288hg38UCSC Ensembl
Innerchr21:15116712..15347609hg19UCSC Ensembl
Innerchr21:14038583..14269480hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38230898
hg19230898
hg18230898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586452
Samples
Known GenesANKRD20A11P, C21orf15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059465
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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