A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1918



Internal ID15546481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:87507427..87552439hg38UCSC Ensembl
Outerchr16:87541033..87586045hg19UCSC Ensembl
Outerchr16:86098534..86143546hg18UCSC Ensembl
Outerchr16:86098534..86143546hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3845013
hg1945013
hg1845013
hg1745013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7291
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)nsv1918
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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