A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259854



Internal ID20826894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141935686..141936916hg38UCSC Ensembl
chr3:141654528..141655758hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571338
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259854
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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