A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249330



Internal ID20816370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223520862..223521660hg38UCSC Ensembl
chr1:223694204..223695002hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537977
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249330
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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