A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262441



Internal ID20829481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123190374..123190979hg38UCSC Ensembl
chr3:122909221..122909826hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566430
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262441
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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