A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590997



Internal ID16378406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95147113..95199680hg38UCSC Ensembl
Innerchr3:94865957..94918524hg19UCSC Ensembl
Innerchr3:96348647..96401214hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3852568
hg1952568
hg1852568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8445n54
Supporting Variantsnssv967791
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590997
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