A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009374



Internal ID18751905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25597903..25644313hg38UCSC Ensembl
Innerchr3:25639394..25685804hg19UCSC Ensembl
Innerchr3:25614398..25660808hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3846411
hg1946411
hg1846411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4707n100
Supporting Variantsnssv3589513
Samples
Known GenesRARB, TOP2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009374
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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