A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059387



Internal ID19148606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17333717..17398509hg38UCSC Ensembl
Innerchr21:18706036..18770828hg19UCSC Ensembl
Innerchr21:17627907..17692699hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3864793
hg1964793
hg1864793
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599674
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)nsv1059387
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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