A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015245



Internal ID21924588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154125789..154126102hg38UCSC Ensembl
chr6:154446924..154447237hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573985
Samples
Known GenesOPRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015245
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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