A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1808



Internal ID15546371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:52180867..52213284hg38UCSC Ensembl
Outerchr16:52214779..52247196hg19UCSC Ensembl
Outerchr16:50772280..50804697hg18UCSC Ensembl
Outerchr16:50772280..50804697hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3832418
hg1932418
hg1832418
hg1732418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7251
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)nsv1808
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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