A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591928



Internal ID16379337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144332055..145104249hg38UCSC Ensembl
Innerchr3:144050897..144822081hg19UCSC Ensembl
Innerchr3:145533587..146304771hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38772195
hg19771185
hg18771185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975228
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591928
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer