A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568374



Internal ID20941445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99436590..99437648hg38UCSC Ensembl
chr6:99884466..99885524hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272831
Samples
Known GenesUSP45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568374
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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