A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563083



Internal ID20936154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154055196..154056267hg38UCSC Ensembl
chr6:154376331..154377402hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381072
hg191072
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270045
Samples
Known GenesOPRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563083
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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