A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592764



Internal ID16033487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189639152..189650568hg38UCSC Ensembl
Innerchr3:189356941..189368357hg19UCSC Ensembl
Innerchr3:190839635..190851051hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3811417
hg1911417
hg1811417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv982906, nssv982907
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592764
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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