A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587320



Internal ID16374729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:24340506..24408437hg38UCSC Ensembl
Innerchr21:25712819..25780751hg19UCSC Ensembl
Innerchr21:24634690..24702622hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3867932
hg1967933
hg1867933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946576
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587320
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