A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516084



Internal ID15096691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154027470..154039662hg38UCSC Ensembl
Innerchr6:154348605..154360797hg19UCSC Ensembl
Innerchr6:154390298..154402490hg18UCSC Ensembl
Innerchr6:154440719..154452911hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3812193
hg1912193
hg1812193
hg1712193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692458, nssv692764, nssv666111
Samples
Known GenesOPRM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516084
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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