A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587059



Internal ID16374468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:15216094..15228088hg38UCSC Ensembl
Innerchr21:16588414..16600408hg19UCSC Ensembl
Innerchr21:15510285..15522279hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3811995
hg1911995
hg1811995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv945469
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587059
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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