A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598567



Internal ID20971638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29484491..29484986hg38UCSC Ensembl
chr22:29880480..29880975hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255491
Samples
Known GenesNEFH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598567
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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