A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831278



Internal ID6157002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:30916984..31070906hg19UCSC Ensembl
Outerchr8:31036526..31190448hg18UCSC Ensembl
Outerchr8:31036526..31190448hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1447013, nssv1447012
Samples
Known GenesWRN
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831278
Frequency
Sample Size95
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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