A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586983



Internal ID16374392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10324453..10326144hg38UCSC Ensembl
Innerchr21:11186313..11188004hg19UCSC Ensembl
Innerchr21:10208184..10209875hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg381692
hg191692
hg181692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7750n54
Supporting Variantsnssv944876, nssv944875, nssv944877
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586983
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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