A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831958



Internal ID6157682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:101211061..101411181hg19UCSC Ensembl
Outerchr10:101201051..101401171hg18UCSC Ensembl
Outerchr10:101201051..101401171hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1448696
Samples
Known GenesNKX2-3, SLC25A28
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831958
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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