A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059433



Internal ID18801964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:46609492..46632926hg38UCSC Ensembl
Innerchr21:48029404..48052838hg19UCSC Ensembl
Innerchr21:46853832..46877266hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3823435
hg1923435
hg1823435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4445n100
Supporting Variantsnssv3600339
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)nsv1059433
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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