A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5873



Internal ID15543515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:18386677..18417033hg38UCSC Ensembl
Outerchr20:18367321..18397677hg19UCSC Ensembl
Outerchr20:18315321..18345677hg18UCSC Ensembl
Outerchr20:18315321..18345677hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg388921
hg198921
hg188921
hg178921
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3313
Supporting Variants
SamplesNA19129
Known GenesDZANK1
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)nssv5873
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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