A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262813



Internal ID20829853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49308405..49309047hg38UCSC Ensembl
chr3:49345838..49346480hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549708
Supporting Variants
Samples
Known GenesUSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262813
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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