A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229479



Internal ID20796519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127618389..127619707hg38UCSC Ensembl
chr11:127488284..127489602hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381319
hg191319
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586744
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229479
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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