A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059477



Internal ID19148696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10458823..10643715hg38UCSC Ensembl
Innerchr21:10868742..11053634hg19UCSC Ensembl
Innerchr21:9890613..10075505hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38184893
hg19184893
hg18184893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3585017
Samples
Known GenesBAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059477
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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