A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561187



Internal ID20934258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154953153..154953863hg38UCSC Ensembl
chr5:154332713..154333423hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268765
Samples
Known GenesMRPL22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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