A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526187



Internal ID15106794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:174421143..174474776hg38UCSC Ensembl
Innerchr2:175285871..175339504hg19UCSC Ensembl
Innerchr2:174994117..175047750hg18UCSC Ensembl
Innerchr2:175111378..175165011hg17UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3853634
hg1953634
hg1853634
hg1753634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702449
Samples
Known GenesGPR155, SCRN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526187
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