A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587931



Internal ID16375340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45973354..45992746hg38UCSC Ensembl
Innerchr21:47393268..47412660hg19UCSC Ensembl
Innerchr21:46217696..46237088hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3819393
hg1919393
hg1819393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7919n54
Supporting Variantsnssv949280
Samples
Known GenesCOL6A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587931
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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