A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255018



Internal ID20822058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41752050..41753302hg38UCSC Ensembl
chr22:42148054..42149306hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg381253
hg191253
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598332
Supporting Variants
Samples
Known GenesMEI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255018
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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