A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517547



Internal ID15098154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28781383..28813244hg38UCSC Ensembl
Innerchr1:29107895..29139756hg19UCSC Ensembl
Innerchr1:28980482..29012343hg18UCSC Ensembl
Innerchr1:28928511..28960372hg17UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3831862
hg1931862
hg1831862
hg1731862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3n21
Supporting Variantsnssv682690, nssv652332
Samples
Known GenesOPRD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517547
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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