A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259549



Internal ID20826589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125509444..125510395hg38UCSC Ensembl
chr3:125228288..125229239hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38952
hg19952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559323
Supporting Variants
Samples
Known GenesSNX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259549
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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