A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833991



Internal ID6159715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:44514270..44697347hg19UCSC Ensembl
Outerchr20:43947677..44130754hg18UCSC Ensembl
Outerchr20:43947677..44130754hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1455110
Samples
Known GenesC20orf165, CTSA, MMP9, NCOA5, NEURL2, PCIF1, PLTP, SLC12A5, ZNF335
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833991
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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