A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833990



Internal ID6159714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:44400149..44575483hg19UCSC Ensembl
Outerchr20:43833556..44008890hg18UCSC Ensembl
Outerchr20:43833556..44008890hg17UCSC 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 StatusM
Merged Variants
Supporting Variantsnssv1455109, nssv1455108
Samples
Known GenesACOT8, C20orf165, CTSA, DNTTIP1, NEURL2, PCIF1, PLTP, SNX21, TNNC2, UBE2C, WFDC3, ZSWIM1, ZSWIM3
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833990
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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