A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2895200



Internal ID15340987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189646285..189820797hg38UCSC Ensembl
Innerchr3:189364074..189538586hg19UCSC Ensembl
Innerchr3:190846768..191021280hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38174513
hg19174513
hg18174513
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514191
Supporting Variants
SamplesNA18622
Known GenesTP63
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2895200
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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