A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591211



Internal ID20964282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93475839..93476467hg38UCSC Ensembl
chr12:93869615..93870243hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229692
Samples
Known GenesMRPL42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591211
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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