A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262918



Internal ID20829958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72865398..72866124hg38UCSC Ensembl
chr3:72914549..72915275hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546098
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262918
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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