A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9366



Internal ID15540317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:48498089..48524169hg38UCSC Ensembl
Outerchr20:47126335..47140707hg19UCSC Ensembl
Outerchr20:46559742..46574114hg18UCSC Ensembl
Outerchr20:46559742..46574114hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3813473
hg1913473
hg1813473
hg1713473
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3406
Supporting Variants
SamplesNA18517
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)nssv9366
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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