A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255057



Internal ID20822097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44617664..44619230hg38UCSC Ensembl
chr22:45013544..45015110hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381567
hg191567
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596846
Supporting Variants
Samples
Known GenesLINC00229
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255057
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00032


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