A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573985



Internal ID21766028
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 StatusS
Merged Variantsnsv6015245
Supporting Variants
Samples
Known GenesOPRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573985
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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