A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586883



Internal ID16374292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10644023..10813996hg38UCSC Ensembl
Innerchr21:10698461..10868434hg19UCSC Ensembl
Innerchr21:9720332..9890305hg18UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38169974
hg19169974
hg18169974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7727n54
Supporting Variantsnssv944770, nssv944769, nssv944768
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586883
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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