A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv945516



Internal ID16239472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:16998393..17029806hg38UCSC Ensembl
Innerchr21:18370713..18402124hg19UCSC Ensembl
Innerchr21:17292584..17323995hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3831414
hg1931412
hg1831412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587081
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv945516
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