A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587142



Internal ID16374551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18682124..18706106hg38UCSC Ensembl
Innerchr21:20054442..20078424hg19UCSC Ensembl
Innerchr21:18976313..19000295hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3823983
hg1923983
hg1823983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7779n54
Supporting Variantsnssv1150981
SamplesHGDP00641
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587142
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer