A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6966



Internal ID15551928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:67554784..67588992hg38UCSC Ensembl
Outerchr10:69314542..69348750hg19UCSC Ensembl
Outerchr10:68984548..69018756hg18UCSC Ensembl
Outerchr10:68984548..69018756hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3834209
hg1934209
hg1834209
hg1734209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1899
SamplesNA18555
Known GenesCTNNA3
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)nsv6966
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