A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598861



Internal ID20971932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31710272..31711472hg38UCSC Ensembl
chr22:32106258..32107458hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4686n223
Supporting Variantsnssv18255111
Samples
Known GenesPRR14L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598861
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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