A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592414



Internal ID16379823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163273578..163404224hg38UCSC Ensembl
Innerchr3:162991366..163122012hg19UCSC Ensembl
Innerchr3:164474060..164604706hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38130647
hg19130647
hg18130647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv981068
Samples
Known GenesCT64
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592414
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