A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587561



Internal ID16374970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41687463..41716229hg38UCSC Ensembl
Innerchr21:43107623..43136389hg19UCSC Ensembl
Innerchr21:41980692..42009458hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3828767
hg1928767
hg1828767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7848n54
Supporting Variantsnssv1152408
Samples1780854235_A
Known GenesLINC00111, LINC00479
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587561
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