A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579284



Internal ID20952355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69749686..69750313hg38UCSC Ensembl
chr16:69783589..69784216hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241223
Samples
Known GenesNOB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579284
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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