A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528201



Internal ID15108808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:179862113..179863508hg38UCSC Ensembl
Innerchr1:179831248..179832643hg19UCSC Ensembl
Innerchr1:178097871..178099266hg18UCSC Ensembl
Innerchr1:176562905..176564300hg17UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg381396
hg191396
hg181396
hg171396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704761
Samples
Known GenesTOR1AIP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528201
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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