A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589776



Internal ID20962847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109066530..109067139hg38UCSC Ensembl
chr12:109504335..109504944hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221155
Samples
Known GenesUSP30
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589776
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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