A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573919



Internal ID20946990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99493205..99494656hg38UCSC Ensembl
chr6:99941081..99942532hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381452
hg191452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6337n223
Supporting Variantsnssv18272837
Samples
Known GenesUSP45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573919
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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