A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261989



Internal ID20829029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23905878..23907143hg38UCSC Ensembl
chr3:23947369..23948634hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381266
hg191266
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549677
Supporting Variants
Samples
Known GenesNKIRAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261989
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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