A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587016



Internal ID16374425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13597606..13998542hg38UCSC Ensembl
Innerchr21:14969927..15370863hg19UCSC Ensembl
Innerchr21:13891798..14292734hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38400937
hg19400937
hg18400937
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7757n54
Supporting Variantsnssv944919
Samples
Known GenesANKRD20A11P, C21orf15, LOC100288966, MIR8069, POTED
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587016
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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