A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527049



Internal ID15107656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154058017..154062523hg38UCSC Ensembl
Innerchr6:154379152..154383658hg19UCSC Ensembl
Innerchr6:154420845..154425351hg18UCSC Ensembl
Innerchr6:154471266..154475772hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg384507
hg194507
hg184507
hg174507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703425
Samples
Known GenesOPRM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527049
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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