A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587542



Internal ID16374951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41613178..41618003hg38UCSC Ensembl
Innerchr21:43033338..43038163hg19UCSC Ensembl
Innerchr21:41906407..41911232hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg384826
hg194826
hg184826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7844n54
Supporting Variantsnssv947041, nssv947042
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587542
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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