A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590279



Internal ID16031002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:51690131..51703836hg38UCSC Ensembl
Innerchr3:51724147..51737852hg19UCSC Ensembl
Innerchr3:51699187..51712892hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3813706
hg1913706
hg1813706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8322n54
Supporting Variantsnssv963059
Samples
Known GenesTEX264
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590279
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