A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589700



Internal ID16377109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12286252..12299426hg38UCSC Ensembl
Innerchr3:12327751..12340925hg19UCSC Ensembl
Innerchr3:12302751..12315925hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3813175
hg1913175
hg1813175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959117
Samples
Known GenesPPARG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589700
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