A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1828



Internal ID15546391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:63332934..63377800hg38UCSC Ensembl
Outerchr16:63366838..63411704hg19UCSC Ensembl
Outerchr16:61924339..61969205hg18UCSC Ensembl
Outerchr16:61924339..61969205hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3844867
hg1944867
hg1844867
hg1744867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7259
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)nsv1828
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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