A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5966



Internal ID15543402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:50846253..50898059hg38UCSC Ensembl
Outerchr3:50883684..50935490hg19UCSC Ensembl
Outerchr3:50858688..50910511hg18UCSC Ensembl
Outerchr3:50858688..50910511hg17UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3851807
hg1951807
hg1851824
hg1751824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7353
Supporting Variants
SamplesNA19129
Known GenesDOCK3
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)nssv5966
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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