A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4167



Internal ID15202163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:189638804..189662392hg38UCSC Ensembl
Outerchr3:189356593..189380181hg19UCSC Ensembl
Outerchr3:190839287..190862875hg18UCSC Ensembl
Outerchr3:190839295..190862883hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3823589
hg1923589
hg1823589
hg1723589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2440
SamplesNA18555
Known GenesTP63
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv4167
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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