A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520558



Internal ID15447851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154062523..154097279hg38UCSC Ensembl
Innerchr6:154383658..154418414hg19UCSC Ensembl
Innerchr6:154425351..154460107hg18UCSC Ensembl
Innerchr6:154475772..154510528hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3834757
hg1934757
hg1834757
hg1734757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694388
Samples
Known GenesOPRM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520558
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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