A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833828



Internal ID6159552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39084759..39257979hg19UCSC Ensembl
Outerchr19:43776599..43949819hg18UCSC Ensembl
Outerchr19:43776599..43949819hg17UCSC Ensembl
Cytoband19q13.2
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 Variantsnssv1454704
Samples
Known GenesACTN4, CAPN12, EIF3K, MAP4K1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833828
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