A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831891



Internal ID6157615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:64168907..64343478hg19UCSC Ensembl
Outerchr10:63838913..64013484hg18UCSC Ensembl
Outerchr10:63838913..64013484hg17UCSC Ensembl
Cytoband10q21.2
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 Variantsnssv1448545
Samples
Known GenesZNF365
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831891
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