A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1833



Internal ID15546396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:65325030..65369897hg38UCSC Ensembl
Outerchr16:65358933..65403800hg19UCSC Ensembl
Outerchr16:63916434..63961301hg18UCSC Ensembl
Outerchr16:63916434..63961301hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3844868
hg1944868
hg1844868
hg1744868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7260
SamplesNA12156
Known GenesLINC00922
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)nsv1833
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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