A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013411



Internal ID18755942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189645877..189658601hg38UCSC Ensembl
Innerchr3:189363666..189376390hg19UCSC Ensembl
Innerchr3:190846360..190859084hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3812725
hg1912725
hg1812725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3611326
Samples
Known GenesTP63
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013411
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