A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4659



Internal ID15196533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:16752452..16797083hg38UCSC Ensembl
Outerchr20:16733097..16777728hg19UCSC Ensembl
Outerchr20:16681097..16725728hg18UCSC Ensembl
Outerchr20:16681097..16725728hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3844632
hg1944632
hg1844632
hg1744632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3306
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)nssv4659
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer