A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264017



Internal ID20831057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68989466..68990360hg38UCSC Ensembl
chr3:69038617..69039511hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38895
hg19895
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536015
Supporting Variants
Samples
Known GenesEOGT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264017
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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