A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv459854



Internal ID15519919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25303640..25514700hg38UCSC Ensembl
Innerchr22:25699607..25910667hg19UCSC Ensembl
Innerchr22:24029607..24240667hg18UCSC Ensembl
Innerchr22:24024161..24235221hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38211061
hg19211061
hg18211061
hg17211061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv575n27
Supporting Variantsnssv536524
Samples1798860565_A
Known GenesCRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)nsv459854
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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