A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2126



Internal ID15194723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:838602..849476hg38UCSC Ensembl
Outerchr16:888602..899476hg19UCSC Ensembl
Outerchr16:828603..839477hg18UCSC Ensembl
Outerchr16:828603..839477hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810030
hg1910030
hg1810030
hg1710030
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1704
Supporting Variants
SamplesNA18555
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)nssv2126
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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