A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262858



Internal ID20829898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69235508..69236340hg38UCSC Ensembl
chr3:69284659..69285491hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554556
Supporting Variants
Samples
Known GenesFRMD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262858
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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