A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1916



Internal ID15546479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:86797431..86842753hg38UCSC Ensembl
Outerchr16:86831037..86876359hg19UCSC Ensembl
Outerchr16:85388538..85433860hg18UCSC Ensembl
Outerchr16:85388538..85433860hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3845323
hg1945323
hg1845323
hg1745323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7288
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)nsv1916
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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