A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593060



Internal ID20966131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110497857..110498011hg38UCSC Ensembl
chr12:110935662..110935816hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226826
Samples
Known GenesVPS29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593060
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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