A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694388



Internal ID15431040
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520558
Supporting Variants
Samples
Known GenesOPRM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694388
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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