A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5592



Internal ID15543854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:18810573..18832773hg38UCSC Ensembl
Outerchr16:18821895..18844095hg19UCSC Ensembl
Outerchr16:18729396..18751596hg18UCSC Ensembl
Outerchr16:18729396..18751596hg17UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3822201
hg1922201
hg1822201
hg1722201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1752
Supporting Variants
SamplesNA19129
Known GenesSMG1
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)nssv5592
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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