A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516668



Internal ID15443961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189809388..189815361hg38UCSC Ensembl
Innerchr3:189527177..189533150hg19UCSC Ensembl
Innerchr3:191009871..191015844hg18UCSC Ensembl
Innerchr3:191009879..191015852hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg385974
hg195974
hg185974
hg175974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673111, nssv670028
Samples
Known GenesTP63
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516668
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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