A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598344



Internal ID20971415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42013399..42014051hg38UCSC Ensembl
chr22:42409403..42410055hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255024
Samples
Known GenesWBP2NL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598344
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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