A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5882



Internal ID15543504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:47829750..47840023hg38UCSC Ensembl
Outerchr20:46458494..46468767hg19UCSC Ensembl
Outerchr20:45891901..45902174hg18UCSC Ensembl
Outerchr20:45891901..45902174hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg389742
hg199742
hg189742
hg179742
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3399
Supporting Variants
SamplesNA19129
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)nssv5882
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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