A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254881



Internal ID20821921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17523757..17524411hg38UCSC Ensembl
chr22:18002784..18003458hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38655
hg19675
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597679
Supporting Variants
Samples
Known GenesCECR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254881
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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