A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260696



Internal ID20827736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43334041..43334713hg38UCSC Ensembl
chr3:43375533..43376205hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553875
Supporting Variants
Samples
Known GenesSNRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260696
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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