A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4206



Internal ID15538933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:26169089..26178748hg38UCSC Ensembl
Outerchr16:26180410..26190069hg19UCSC Ensembl
Outerchr16:26087911..26097570hg18UCSC Ensembl
Outerchr16:26087911..26097570hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg384857
hg194857
hg184857
hg174857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1771
Supporting Variants
SamplesNA12878
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)nssv4206
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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