A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249509



Internal ID20816549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183639250..183640116hg38UCSC Ensembl
chr1:183608385..183609251hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549483
Supporting Variants
Samples
Known GenesRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249509
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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