A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1864



Internal ID15546427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:72064069..72084058hg38UCSC Ensembl
Outerchr16:72097968..72117957hg19UCSC Ensembl
Outerchr16:70655469..70675458hg18UCSC Ensembl
Outerchr16:70655469..70675458hg17UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3817599
hg1917599
hg1817599
hg1717599
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9317, nssv1319
SamplesNA18517, NA19240
Known GenesHPR
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)nsv1864
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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