A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139138



Internal ID20706178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154125795..154126102hg38UCSC Ensembl
chr6:154446930..154447237hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600854
Supporting Variants
Samples
Known GenesOPRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.87049


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