A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561078



Internal ID20934149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131478692..131479580hg38UCSC Ensembl
chr3:131197536..131198424hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260240
Samples
Known GenesMRPL3, SNORA58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561078
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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