A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564490



Internal ID20937561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106932976..106934219hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381244
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564490
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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