A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563283



Internal ID20936354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83497722..83901118hg38UCSC Ensembl
chr6:84207441..84610837hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg38403397
hg19403397
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274792
Samples
Known GenesCYB5R4, PRSS35, RIPPLY2, SNAP91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563283
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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