A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255603



Internal ID20822643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40883082..40883226hg38UCSC Ensembl
chr22:41279086..41279230hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598347
Supporting Variants
Samples
Known GenesXPNPEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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