A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518281



Internal ID15445574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:235205409..235215911hg38UCSC Ensembl
Innerchr2:236114053..236124555hg19UCSC Ensembl
Innerchr2:235778792..235789294hg18UCSC Ensembl
Innerchr2:235896053..235906555hg17UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3810503
hg1910503
hg1810503
hg1710503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695712
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518281
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