A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590151



Internal ID16377560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:43286329..43287037hg38UCSC Ensembl
Innerchr3:43327821..43328529hg19UCSC Ensembl
Innerchr3:43302825..43303533hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38709
hg19709
hg18709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8298n54
Supporting Variantsnssv962436
Samples
Known GenesSNRK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590151
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