A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590808



Internal ID16378217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:83092451..83256297hg38UCSC Ensembl
Innerchr3:83141602..83305448hg19UCSC Ensembl
Innerchr3:83224292..83388138hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38163847
hg19163847
hg18163847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967071, nssv967070
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590808
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