A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565361



Internal ID20938432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111800850..111801628hg38UCSC Ensembl
chr6:112122053..112122831hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38779
hg19779
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268503
Samples
Known GenesFYN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565361
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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