A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591585



Internal ID16032308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127667659..127702011hg38UCSC Ensembl
Innerchr3:127386502..127420854hg19UCSC Ensembl
Innerchr3:128869192..128903544hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3834353
hg1934353
hg1834353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151795
SamplesHGDP00402
Known GenesABTB1, MGLL, PODXL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591585
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