A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11036



Internal ID15192986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:38841749..38872058hg38UCSC Ensembl
Outerchr20:37470392..37500701hg19UCSC Ensembl
Outerchr20:36903806..36934115hg18UCSC Ensembl
Outerchr20:36903806..36934115hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg389562
hg199562
hg189562
hg179562
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3373
Supporting Variants
SamplesNA15510
Known GenesPPP1R16B
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)nssv11036
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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