A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262826



Internal ID20829866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49472526..49474352hg38UCSC Ensembl
chr3:49509959..49511785hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381827
hg191827
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545383
Supporting Variants
Samples
Known GenesDAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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