A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259686



Internal ID20826726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136849410..136849999hg38UCSC Ensembl
chr3:136568252..136568841hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556098
Supporting Variants
Samples
Known GenesSLC35G2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259686
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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