A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592854



Internal ID16380263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191678183..191713707hg38UCSC Ensembl
Innerchr3:191395972..191431496hg19UCSC Ensembl
Innerchr3:192878666..192914190hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3835525
hg1935525
hg1835525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153415
Samples1780854436_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592854
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