A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264019



Internal ID20831059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69026620..69027017hg38UCSC Ensembl
chr3:69075771..69076168hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545128
Supporting Variants
Samples
Known GenesTMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264019
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00048


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