A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587051



Internal ID16374460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:15215157..15216815hg38UCSC Ensembl
Innerchr21:16587477..16589135hg19UCSC Ensembl
Innerchr21:15509348..15511006hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381659
hg191659
hg181659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944955
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587051
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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