A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587634



Internal ID16028357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42502887..42514449hg38UCSC Ensembl
Innerchr21:43922997..43934559hg19UCSC Ensembl
Innerchr21:42796066..42807628hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3811563
hg1911563
hg1811563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv947357
Samples
Known GenesSLC37A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587634
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