A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv949284



Internal ID16243240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45989589..46068473hg38UCSC Ensembl
Innerchr21:47409503..47488387hg19UCSC Ensembl
Innerchr21:46233931..46312815hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3878885
hg1978885
hg1878885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587935
Supporting Variants
Samples
Known GenesCOL6A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv949284
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