A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526675



Internal ID15453968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:228426927..228480036hg38UCSC Ensembl
Innerchr2:229291643..229344752hg19UCSC Ensembl
Innerchr2:228999887..229052996hg18UCSC Ensembl
Innerchr2:229117148..229170257hg17UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3853110
hg1953110
hg1853110
hg1753110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703007
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526675
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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