A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7834



Internal ID15536030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:83090943..83135897hg38UCSC Ensembl
Outerchr3:83140094..83185048hg19UCSC Ensembl
Outerchr3:83222784..83267738hg18UCSC Ensembl
Outerchr3:83222784..83267738hg17UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3844955
hg1944955
hg1844955
hg1744955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3895
Supporting Variants
SamplesNA12156
Known Genes
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)nssv7834
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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