A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261965



Internal ID20829005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22709629..22741122hg38UCSC Ensembl
chr3:22751120..22782613hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3831494
hg1931494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261965
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00096


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